China food production license
Hunan market-regulation authority. License SC13043011210578; special dietary food category. Source copy states validity through 5 February 2031.
Quality records & company documents
Review JWAY BIO manufacturing documents, food production license, third-party assessment, product safety reports and batch COA requirements.
Quality review starts with an approved specification and follows the material lots, manufacturing record and finished pack. The company-provided documents below support buyer review of the manufacturing entity; product-specific evidence is agreed for the order.
Company document library
Third-party cGMP assessment
Technical Standards Institute (TSI), certificate TGM/CN48/1231208. Source copy states validity through 11 May 2029. This is a third-party assessment document.
Food facility registration document
Company-supplied registration-service document. This is not an FDA-issued certificate and does not establish product approval. Request current status during procurement.
FDA food facility registration does not convey FDA approval or endorsement of a facility or its products. FDA does not issue food-facility registration certificates. Read the scope and issuer of third-party and registration-service documents accurately.
Product & transport documents
- Oral pouch GHS safety data sheetCompany source document · PDF · specific report scope applies
- Air transport assessmentCompany source document · PDF · confirm applicability to the actual shipment
Agree the order’s release record
- Approved formula, product specification and relevant test methods
- Raw-material lot identification and supplier records
- In-process checks for the agreed pouch and pack attributes
- Finished-product batch COA with the agreed test scope
- Commercial invoice, packing list and shipment-specific records
Make the buyer review specific
Tell the team which procurement standards and documents your organization requires. A general certificate library cannot replace the product, facility and market review for your particular order. Request current copies and identify any additional testing before the quotation is finalized.
Read the guide to COA and batch release · Discuss your document requirements
Build a well-defined product
Talk to the project team
Share your market, formula direction, flavor and packaging requirements.
- Private label & OEM / ODM
- Formulation & sampling
- Manufacturing & documents