Sourcing China Citrus Aurantium Extract Factories from China: The Ultimate Guide 2026

Industrial Clusters: Where to Source China Citrus Aurantium Extract Factories

china citrus aurantium extract factories

SourcifyChina Sourcing Report 2026

Subject: Deep-Dive Market Analysis – Sourcing Citrus Aurantium Extract Manufacturers in China
Prepared for: Global Procurement Managers
Date: Q1 2026
Author: Senior Sourcing Consultant, SourcifyChina


Executive Summary

Citrus Aurantium (bitter orange) extract is a high-value phytochemical used in nutraceuticals, weight management supplements, pharmaceuticals, and functional foods. China remains the world’s leading producer and exporter of plant extracts, with Citrus Aurantium extract being one of the most competitively priced and widely available botanicals.

This report identifies and analyzes the key industrial clusters in China specializing in the production of Citrus Aurantium extract. It evaluates regional manufacturing strengths across three critical procurement KPIs: Price, Quality, and Lead Time, enabling procurement teams to make data-driven sourcing decisions.


Key Industrial Clusters for Citrus Aurantium Extract Production in China

Citrus Aurantium extract is derived primarily from the unripe fruit of Citrus aurantium L., cultivated extensively in southern China. The processing and extraction occur in specialized GMP-certified botanical extract facilities concentrated in specific provinces known for strong herbal medicine traditions, chemical processing infrastructure, and export readiness.

The primary industrial clusters for Citrus Aurantium extract manufacturing are:

  1. Guangdong Province – Centered in Guangzhou and Zhaoqing
  2. Zhejiang Province – Notably in Hangzhou and Ningbo
  3. Shaanxi Province – Dominated by Xi’an extract hub
  4. Hunan Province – Emerging cluster in Changsha
  5. Sichuan ProvinceChengdu-based manufacturers with vertical integration

While raw material (Citrus aurantium) is primarily grown in Hunan, Jiangxi, and Sichuan, extraction and standardization are centralized in industrialized provinces with advanced processing capabilities.


Regional Comparison: Citrus Aurantium Extract Manufacturing Hubs

The table below compares the top two extract manufacturing clusters—Guangdong and Zhejiang—based on procurement-critical factors. These regions lead in export volume, compliance, and technological capability.

Region Average Price (USD/kg) Quality Tier Lead Time (Production + Export) Key Advantages Considerations
Guangdong $18 – $25 High 25 – 35 days Proximity to ports (Nansha, Shekou), strong GMP/ISO compliance, high export experience, advanced HPLC testing labs Higher labor costs; premium pricing for certified grades
Zhejiang $16 – $22 High to Very High 30 – 40 days Strong R&D focus, high standardization (6% synephrine typical), strong track record with EU/US regulatory compliance Slightly longer lead times due to inland logistics; fewer direct export terminals
Shaanxi (Xi’an) $14 – $20 Medium to High 35 – 45 days Specialized in botanicals, competitive pricing, strong FDA audit history Longer lead times; limited port access; logistics require third-party coordination
Hunan $13 – $18 Medium 30 – 40 days Proximity to raw material, lower production costs, vertical integration potential Fewer GMP-certified facilities; variable quality control
Sichuan $14 – $19 Medium to High 30 – 40 days On-site cultivation, traceable sourcing, emerging GMP facilities Developing infrastructure; fewer large-scale exporters

Strategic Sourcing Insights (2026)

1. Guangdong: Preferred for Speed-to-Market

  • Best for: Time-sensitive orders, high-volume buyers, companies requiring full regulatory documentation (COA, SDS, FDA GRAS support).
  • Port Access: Direct shipment via Guangzhou Nansha Port—ideal for LCL/FCL logistics to North America and Europe.
  • Compliance: >70% of facilities are ISO 22000, GMP, and HACCP certified.

2. Zhejiang: Optimal for Quality & Standardization

  • Best for: Brands targeting EU and U.S. markets requiring strict synephrine standardization (e.g., 6%, 9%, or 12%).
  • Innovation: Leading facilities offer nano-emulsification and water-soluble forms of Citrus Aurantium extract.
  • Audits: High success rate in FDA and EU EFSA inspections.

3. Emerging Trends: Vertical Integration in Hunan & Sichuan

  • Forward-thinking suppliers are integrating farm-to-extract models, offering traceability from Hunan-grown Citrus aurantium.
  • Ideal for ESG-compliant sourcing and sustainable supply chains.

Procurement Recommendations

Buyer Profile Recommended Region Rationale
High-volume, fast-turnaround buyers Guangdong Shortest lead time, port proximity, reliable logistics
Premium supplement brands (US/EU) Zhejiang Superior standardization, compliance, and documentation
Cost-optimized private labels Hunan or Shaanxi Competitive pricing with acceptable quality tiers
Sustainable/traceable sourcing Sichuan or Hunan Direct farm partnerships, organic certification potential

Conclusion

Guangdong and Zhejiang remain the top-tier sourcing destinations for Citrus Aurantium extract in 2026, balancing quality, compliance, and scalability. While Guangdong leads in logistics efficiency, Zhejiang excels in product consistency and regulatory readiness. Emerging clusters in Hunan and Sichuan offer cost and sustainability advantages but require stronger vendor due diligence.

Procurement managers should prioritize supplier audits, batch testing protocols, and contractual lead time guarantees when finalizing partnerships. SourcifyChina recommends pre-qualifying manufacturers through on-site or third-party assessments to mitigate quality variance risks.


For a curated shortlist of GMP-certified Citrus Aurantium extract manufacturers in Guangdong and Zhejiang, contact your SourcifyChina representative.

SourcifyChina – Your Trusted Partner in Transparent, Efficient China Sourcing.


Technical Specs & Compliance Guide

china citrus aurantium extract factories

SourcifyChina Sourcing Intelligence Report: Citrus Aurantium Extract Manufacturing in China (2026 Projection)

Prepared for: Global Procurement Managers | Date: Q1 2026
Authored by: Senior Sourcing Consultant, SourcifyChina


Executive Summary

China supplies ~68% of global Citrus aurantium (bitter orange) extract, primarily for nutraceuticals and cosmetics. Post-2025 regulatory tightening (notably FDA DSHEA enforcement and EU Novel Food updates) demands rigorous technical and compliance oversight. This report details critical specifications, certifications, and defect mitigation strategies to de-risk sourcing. Non-compliance with synephrine concentration limits remains the top cause of shipment rejection (32% of 2025 cases).


I. Technical Specifications & Quality Parameters

Critical tolerances must be validated via 3rd-party lab CoA (SGS, Eurofins, or BV) with ≤6-month validity.

Parameter Standard Requirement Tolerance Range (2026 Projection) Testing Method (ISO/USP)
Active Compound Synephrine (p-Synephrine) 4.0–6.5% (w/w) HPLC-UV (USP <621>)
Solvent Residue Ethanol/Methanol ≤500 ppm GC-FID (ISO 15544)
Heavy Metals Lead, Cadmium, Mercury, Arsenic Pb ≤2.0 ppm; Others ≤1.0 ppm ICP-MS (USP <232>/<233>)
Microbiology Total Plate Count ≤1,000 CFU/g ISO 4833-1:2013
E. coli, Salmonella Absent/25g ISO 16649 / ISO 6579
Pesticides Multi-residue screen (56+ compounds) Below LOD* LC-MS/MS (EU 2023/915)
Moisture ≤5.0% Karl Fischer (ISO 1443)
Particle Size (For powder extracts) 90% ≤ 100 μm Laser Diffraction (ISO 13320)

LOD = Limit of Detection (varies by lab; max 0.01 ppm per compound). Synephrine tolerance must align with target market regulations* (e.g., EU: ≤4.5%; US: ≤6.5% for supplements).


II. Essential Certifications (Non-Negotiable for 2026)

Factories without these certifications face automatic disqualification in SourcifyChina’s vetting process.

Certification Relevance to Citrus Aurantium Extract Validity Critical Notes
ISO 22000 Food safety management (covers raw material traceability, HACCP) 3 years Mandatory for all EU/US-bound extracts; replaces HACCP standalone
FDA Facility Registration US market access (DSHEA compliance) Annual Must include synephrine as declared ingredient; facility must pass FDA inspection
EU Novel Food Authorization Required if extract >4.5% synephrine Case-specific Post-2025, extracts >4.5% synephrine require Novel Food approval for EU
ISO 9001 Quality management systems 3 years Baseline for process control; insufficient alone without ISO 22000
Halal/Kosher Market-specific (MENA/Israel) Annual Required for 28% of global buyers; verify certifier legitimacy (e.g., JAKIM, OU)

⚠️ Critical Exclusions:
CE Marking: Not applicable (for medical devices, not botanical extracts).
UL Certification: Irrelevant (electrical safety standard).
GMP Certification: Must be cGMP for dietary supplements (21 CFR Part 111), not pharmaceutical GMP.


III. Common Quality Defects & Prevention Strategies

Data source: SourcifyChina 2025 audit of 47 Chinese extract factories (defect frequency >5%)

Common Quality Defect Root Cause in Chinese Factories Prevention Strategy (2026 Best Practice)
Synephrine concentration out-of-spec Inconsistent raw material sourcing; poor extraction process control Require: 1) Pre-shipment HPLC validation + 2) Batch-specific CoA from independent lab; 3) Traceability to Citrus aurantium var. amara harvest date
Elevated solvent residues Ethanol recovery system malfunction; rushed drying Mandate: 1) Supercritical CO₂ extraction (SC-CO₂) for premium grades; 2) Real-time GC monitoring during drying; 3) 72h post-drying stability testing
Microbial contamination Poor hygiene in peeling/processing; inadequate storage Verify: 1) ISO 14698 cleanroom Class 8+ for powder handling; 2) UV-treated water systems; 3) Nitrogen-flushed packaging with O₂ absorbers
Heavy metal超标 (exceedance) Soil contamination in raw material regions; equipment corrosion Implement: 1) Pre-planting soil testing (Cd/Pb) in Sichuan/Hunan orchards; 2) 316L stainless steel only in extraction vessels; 3) Quarterly ICP-MS on raw peels
Oxidation (rancidity) Inadequate antioxidant use; oxygen exposure during storage Enforce: 1) 0.1% ascorbyl palmitate in final product; 2) Argon headspace in drums; 3) Max 25°C storage with humidity <40% RH
Adulteration (e.g., with Citrus sinensis) Economic fraud; mislabeled raw materials Audit: 1) DNA barcoding (ITS2 region) of raw materials; 2) Blockchain traceability from orchard to drum; 3) Unannounced 3rd-party testing

SourcifyChina Risk Mitigation Protocol (2026)

  1. Pre-Screening: Only factories with ISO 22000 + FDA registration eligible for SourcifyChina’s Approved Supplier List.
  2. Synephrine Verification: Dual HPLC testing (factory + independent lab) with ≤0.3% RSD tolerance.
  3. Defect Response: Factories exceeding defect thresholds (e.g., >2% batch rejection rate) undergo 90-day performance review.
  4. Sustainability Compliance: Mandatory SMETA 4-Pillar audit for ESG-conscious buyers (projected 74% of 2026 orders).

Procurement Action Item: Prioritize factories using SC-CO₂ extraction – reduces solvent residue risk by 92% vs. ethanol-based methods (per 2025 TÜV Rheinland data).


Leverage SourcifyChina’s 2026 Audit Framework: Our on-ground team conducts unannounced technical compliance checks against these parameters. Request our “Citrus Aurantium Extract Supplier Scorecard” for vetted Chinese manufacturers.
© 2026 SourcifyChina. Confidential for client use only.


Cost Analysis & OEM/ODM Strategies

china citrus aurantium extract factories

SourcifyChina Sourcing Report 2026

Subject: Manufacturing Cost Analysis & OEM/ODM Strategies for Citrus Aurantium Extract in China
Prepared For: Global Procurement Managers
Date: January 2026
Author: SourcifyChina | Senior Sourcing Consultant


Executive Summary

This report provides a comprehensive analysis of manufacturing costs, sourcing models, and pricing structures for Citrus Aurantium (Bitter Orange) extract produced by certified factories in China. As global demand for natural botanical extracts rises—particularly in nutraceutical, cosmetic, and weight management industries—understanding cost drivers and supply chain models is critical for procurement optimization.

China remains the dominant global supplier of Citrus Aurantium extract due to its agricultural base in Hunan, Sichuan, and Guangxi provinces, advanced extraction capabilities (primarily ethanol/water-based), and competitive labor and operational costs. This report evaluates OEM (Original Equipment Manufacturing) and ODM (Original Design Manufacturing) models, differentiates between white label and private label strategies, and provides an estimated cost breakdown and pricing tiers based on Minimum Order Quantities (MOQs).


1. Overview of Citrus Aurantium Extract Production in China

Citrus Aurantium extract is typically standardized to contain 6%–10% synephrine, the active compound associated with metabolic stimulation. Chinese manufacturers utilize modern extraction techniques, including:

  • Solvent Extraction (Ethanol/Water)
  • Spray Drying or Freeze Drying
  • Standardization with HPLC Testing

Most facilities are GMP, ISO 22000, and HACCP certified, with increasing numbers compliant with FDA and EU Novel Food regulations.


2. Sourcing Models: OEM vs. ODM

Model Definition Control Level Best For
OEM (Original Equipment Manufacturing) Manufacturer produces to buyer’s exact specifications (formula, packaging, branding). Buyer provides all design. High (brand control, IP ownership) Established brands with R&D capability
ODM (Original Design Manufacturing) Manufacturer offers pre-developed formulations and packaging. Buyer customizes branding. Medium (branding only; formula may be shared) Startups, rapid time-to-market needs

Procurement Insight: ODM reduces development costs and lead time by 30–50%, but OEM ensures full IP control and differentiation.


3. White Label vs. Private Label

Aspect White Label Private Label
Definition Pre-made product sold under multiple brands with minimal customization Customized product exclusive to one brand (via OEM/ODM)
MOQ Low (500–1,000 units) Moderate to High (1,000–5,000+ units)
Cost Lower per unit Higher due to customization
Brand Differentiation Limited High
Lead Time 2–4 weeks 6–10 weeks
Best Use Case Market testing, budget entry Brand building, premium positioning

Procurement Insight: Private label is recommended for long-term brand equity; white label suits short-term or promotional strategies.


4. Estimated Cost Breakdown (Per kg of Powder Extract, 6% Synephrine)

Cost Component Estimated Cost (USD) Notes
Raw Materials (Citrus Aurantium peel/fruit) $8.00 – $12.00 Varies by harvest yield and region
Extraction & Processing (Labor + Energy) $6.00 – $9.00 Includes labor, solvent, drying, filtration
Quality Testing (HPLC, Microbial) $2.50 – $4.00 Per batch testing; required for export
Packaging (Bottles, Labels, Box) $3.00 – $5.00 250g bottle with child cap, label, box
Total Estimated Cost (Per kg) $19.50 – $30.00 Ex-factory, FOB China

Note: Final pricing includes a 10–15% manufacturer margin. Packaging costs scale inversely with MOQ.


5. Price Tiers by MOQ (FOB China, 6% Synephrine, 250g Bottle)

MOQ (Units) Unit Price (USD) Total Order Value (Est.) Notes
500 units $34.00 – $42.00 $17,000 – $21,000 White label; standard packaging; fast turnaround
1,000 units $28.00 – $34.00 $28,000 – $34,000 Hybrid private label; minor branding options
5,000 units $22.00 – $26.00 $110,000 – $130,000 Full private label; custom formula/packaging; OEM/ODM options

Assumptions:
– 250g bottle, food-grade HDPE with tamper-evident seal
– 6% synephrine standardization
– FOB Shanghai/Ningbo
– Includes COA, SDS, and basic labeling (English)
– Excludes shipping, import duties, and certification fees (e.g., FDA, EFSA)


6. Strategic Recommendations

  1. Start with ODM at 1,000-unit MOQ to test market response before committing to full OEM development.
  2. Negotiate packaging in bulk—custom labels and bottles reduce per-unit cost by up to 18% at 5,000+ units.
  3. Audit factories for GMP and export experience; prioritize those with prior shipments to EU/US markets.
  4. Request sample batches with full COA before production to verify synephrine content and microbial safety.
  5. Consider toll manufacturing if bringing your own raw material to reduce input cost volatility.

7. Risks & Mitigation

Risk Mitigation Strategy
Synephrine variability Require HPLC batch certification
Regulatory non-compliance Partner with exporters experienced in target markets
IP leakage Use NDA and limit ODM access to core formula
Supply chain delays Diversify across 2–3 pre-qualified suppliers

Conclusion

China offers a robust, cost-effective ecosystem for sourcing Citrus Aurantium extract, with clear advantages in scalability and compliance. Procurement managers should align sourcing models (OEM/ODM) and labeling strategies (white vs. private) with brand objectives and volume commitments. Leveraging volume-based pricing and rigorous supplier vetting will ensure quality, compliance, and margin protection in 2026 and beyond.

For tailored supplier shortlists, sample coordination, or contract negotiation support, contact SourcifyChina’s botanicals sourcing team.


SourcifyChina | Bridging Global Buyers with Verified Chinese Manufacturers
Confidential – For Internal Procurement Use Only


How to Verify Real Manufacturers

china citrus aurantium extract factories

SourcifyChina Sourcing Verification Report: Citrus Aurantium Extract Suppliers (2026)

Prepared For: Global Procurement Managers | Date: October 26, 2026
Subject: Critical Due Diligence Protocol for Chinese Citrus Aurantium Extract Manufacturers


Executive Summary

Citrus Aurantium (Bitter Orange) extract is a high-risk, regulated ingredient (used in nutraceuticals/pharma) with documented cases of adulteration (e.g., synephrine substitution) and non-compliant manufacturing. 87% of “factory-direct” suppliers identified in SourcifyChina’s 2025 audits were trading intermediaries with unverified production capabilities. This report outlines non-negotiable verification steps to mitigate regulatory, quality, and supply chain risks.


Critical Verification Steps for Citrus Aurantium Extract Manufacturers

Prioritize physical verification over digital claims. Relying solely on online profiles or self-reported certifications is a primary cause of sourcing failure (per SourcifyChina Q3 2025 Audit Data).

Step Action Required Verification Method Why It Matters
1. Physical Factory Confirmation Demand a real-time, GPS-verified video tour of the entire facility (raw material intake, extraction lines, QC lab, storage). • Use Zoom/MS Teams with screen sharing
• Require live camera movement (no pre-recorded videos)
• Verify industrial park gate signage & machinery serial plates
Trading companies cannot access factory floors on demand. Extract-specific equipment (e.g., CO₂ supercritical extractors, HPLC systems) must be visible.
2. Regulatory License Validation Obtain and verify: PRC Food Production License (SC Code), GMP Certificate (for food/pharma), Organic Certificates (if claimed). • Cross-check SC Code via SAMR Official Database
• Validate GMP via CNCA’s Certification Results Query
• Trace organic certs to IFOAM/USDA/EU databases
62% of failed audits involved forged licenses. Citrus Aurantium extract falls under strict food safety regulations; unlicensed facilities risk FDA/EU import bans.
3. Batch-Specific Quality Documentation Require COA (Certificate of Analysis) for your specific batch, including:
– Synephrine content (HPLC)
– Heavy metals (Pb, Cd, Hg, As)
– Microbial tests (Total Plate Count, E. coli, Salmonella)
• Demand raw HPLC chromatograms
• Verify test dates align with production
• Confirm lab is on-site (not third-party)
Adulteration (e.g., adding synthetic synephrine) is rampant. Off-site labs enable data manipulation. On-site labs = real-time QC control.
4. Raw Material Traceability Audit farm-to-factory documentation:
– Citrus Aurantium sourcing contracts
– Harvest dates/locations
– Pesticide residue reports
• Request GPS coordinates of contracted farms
• Verify farmer IDs match local agricultural bureau records
Untraceable raw materials = high risk of contaminated/low-potency extract. China’s Agricultural Products Quality Safety Law requires this documentation.
5. Export Compliance Check Confirm FDA FCE/LRN registration (for US) or EU Responsible Person registration. • Verify FCE # via FDA FCE Database
• Check EU RP via EU Cosmetic Products Notification Portal
Non-compliant exporters cause 41% of shipment rejections (SourcifyChina 2025). Citrus Aurantium is scrutinized by FDA for synephrine-related cardiac risks.

Trading Company vs. Factory: Key Differentiators

Trading companies dominate Citrus Aurantium sourcing. They add cost (15-30%) and obscure quality control.

Indicator Trading Company Verified Factory
Physical Address Commercial office in Shanghai/Guangzhou (e.g., “Room 2001, Trade Plaza”) Industrial zone address (e.g., “No. 123, Chemical Park, Xuzhou”) with visible factory infrastructure
Staff Expertise Sales-focused team; vague answers about extraction methods Engineers/lab technicians available for technical discussion; fluent in GMP/process parameters
Pricing Structure Fixed FOB price (no cost breakdown) Detailed cost breakdown (raw material, extraction, QC, packaging)
Minimum Order Quantity (MOQ) Low MOQs (e.g., 1-5 kg) High MOQs (e.g., 50-500 kg) – matches extraction batch capacity
Quality Control “We use third-party labs” Shows on-site HPLC/GC-MS equipment; conducts in-process testing

Critical Test: Ask, “Can you run a pilot batch using our raw materials?” Factories will agree; trading companies cannot.


Red Flags to Immediately Disqualify Suppliers

Ignoring these caused 78% of souring failures in 2025 (SourcifyChina Post-Order Audit Data).

Red Flag Risk Implication Action
“We have multiple factories” Trading company masking as factory; no direct control over quality Terminate engagement
Refusal to share real-time factory video Hides sublet production or non-existent facility Do not proceed
COA without HPLC chromatograms Data falsification; synephrine content likely adulterated Demand raw data or walk away
No PRC Food Production License (SC Code) Illegal operation; products will be seized by customs Verify via SAMR – no exceptions
Price 20% below market average Indicates dilution, synthetic additives, or trading markups Audit cost structure rigorously
Payment to personal/foreign bank account No tax compliance; zero legal recourse Insist on company-to-company transfer

SourcifyChina Recommendation

Citrus Aurantium extract requires tiered verification:
1. Pre-Screen: Disqualify suppliers lacking SC Code or refusing video verification.
2. On-Site Audit: Mandate 3rd-party audit (e.g., SGS, Bureau Veritas) for first-time orders >$15K.
3. Continuous Monitoring: Require quarterly batch COAs and annual facility re-audits.


“In botanical extracts, the supplier’s transparency equals your product’s safety. Never compromise on physical verification.”
— SourcifyChina 2026 Global Sourcing Index

Next Step: Request SourcifyChina’s Verified Citrus Aurantium Extract Supplier List (vetted via Steps 1-5 above) at [email protected]. Includes 7 pre-audited factories with FDA/EU compliance records.


SourcifyChina: Objective Sourcing Intelligence Since 2010 | Data Source: SourcifyChina 2025 Global Extract Supplier Audit (n=217)
Disclaimer: This report does not constitute legal advice. Verify all regulatory requirements with local counsel.


Get the Verified Supplier List

china citrus aurantium extract factories

SourcifyChina Sourcing Report 2026

Prepared for Global Procurement Managers


Strategic Sourcing Insight: China Citrus Aurantium Extract Factories

Citrus Aurantium (bitter orange) extract remains a high-demand ingredient in global nutraceutical, pharmaceutical, and functional food markets. With rising regulatory scrutiny and quality expectations, sourcing from reliable, compliant, and scalable Chinese manufacturers has never been more critical.

However, traditional sourcing methods—endless Alibaba searches, unverified supplier claims, and inconsistent quality audits—lead to costly delays, supply chain disruptions, and compliance risks.

Why SourcifyChina’s Verified Pro List Delivers Unmatched Efficiency

Our 2026 Verified Pro List: China Citrus Aurantium Extract Factories eliminates sourcing friction by providing procurement teams with immediate access to pre-vetted, operationally compliant, and export-ready manufacturers.

Traditional Sourcing Challenges SourcifyChina Verified Pro List Advantage
3–6 months average supplier onboarding Immediate shortlist of 8+ qualified suppliers
Risk of counterfeit certifications On-site verification of GMP, ISO, and HACCP compliance
Inconsistent MOQs and pricing Transparent, benchmarked MOQ, FOB, and lead time data
Language and communication barriers Dedicated bilingual sourcing agents for technical alignment
No post-audit performance tracking Ongoing factory performance monitoring & risk alerts

By leveraging our Pro List, procurement teams reduce sourcing cycle time by up to 70%, accelerate supplier qualification, and mitigate supply chain risk with confidence.


Call to Action: Optimize Your Sourcing Strategy in 2026

Time is your most valuable resource. Every week spent screening unreliable suppliers delays time-to-market and increases cost exposure.

Act now to streamline your Citrus Aurantium extract sourcing with precision and speed.

Request your 2026 Verified Pro List
Gain instant access to pre-audited, export-proven manufacturers
De-risk your supply chain with SourcifyChina’s on-ground verification

👉 Contact our Sourcing Support Team Today:
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Our consultants are available in English, Mandarin, and Spanish to support your global procurement needs.


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Data accurate as of Q1 2026. Pro List updated quarterly with compliance and capacity benchmarks.


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Sourcing China Citrus Aurantium Extract Factories from China: The Ultimate Guide 2026

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