At Hekona, we firmly believe that true “Finished Product Assurance” stems from meticulous oversight and unwavering commitment to every detail across the entire production chain. We guarantee product quality through rigorous standards and a transparent commitment.
Every finished batch undergoes screening for heavy metals, pesticide residues, microbiological contaminants, and unauthorized additives, with safety metrics far exceeding industry standards.
All active ingredients are verified using precision instruments like High-Performance Liquid Chromatography (HPLC), ensuring the label-claimed potency matches the actual content.
Accelerated stability testing is conducted to determine shelf life, alongside strict testing of physical parameters such as disintegration time and blend uniformity, guaranteeing consistent performance throughout the product’s lifespan.
Prior to final packaging, all products undergo rigorous sampling and testing, including checks for fill weight variation, disintegration time, and microbiological limits.
All approved products are bottled, sealed, and packaged on fully automatic counting and filling lines. The entirely automated process minimizes manual handling and contamination risks.
Product labels clearly display key information, including dosage, active ingredient content, expiration date, and lot number.
Tamper-evident seals are applied to ensure product integrity and safety during transit and storage.
We conduct final inspections on sealing and labeling before shipping products to customers or distributors. Strict adherence to cGMP and FDA standards is maintained throughout production, with complete batch documentation ensuring end-to-end traceability and recall readiness.
Final Quality Inspection：We conduct a final inspection to verify that capsules are properly sealed and labels are intact and correctly applied.
Delivery：Upon successful completion of inspection, products are prepared for final packaging and shipped to the customer or designated distribution center.
Regulatory Compliance: Throughout the entire manufacturing process, we strictly adhere to cGMP (current Good Manufacturing Practice) standards, applicable regulatory requirements, and FDA guidance.
Batch Records: Comprehensive and detailed documentation is created and maintained for each production batch, ensuring full traceability throughout the product lifecycle. This robust documentation system is critical for the effective management of potential quality incidents and product recalls.
In our in-house testing laboratory: Equipped with professional instruments (e.g., HPLC, AAS, and microbiological lab), we perform batch-by-batch testing on key parameters for every finished product lot.
Third-Party Verification: We periodically submit products as “blind samples” to authoritative third-party testing organizations (e.g., SGS, Intertek) for independent verification, ensuring the objectivity and impartiality of the test data.
End-to-End Quality Assurance & Compliant Delivery
