Read the holder and production scope first
MITEYO’s supplied document library names Guangdong Come Health Biotechnology Co., Ltd. The Shenzhen office coordinates sales and R&D. The certificate file helps a buying team identify the holder, site, technologies, scope and stated dates for the proposed order. Match those details to the actual producing site and product, rather than collecting logos alone.
The seven supplied records answer different questions
The file contains NSF cGMP, FDA facility-registration verification, HACCP, ISO 22000, IQNET recognition, Halal with product appendices, and a BRCGS FSMA module document. IQNET recognizes the listed ISO food-safety system; it is not a second product standard. The BRCGS record should be described by its stated module and scope. The supplied NSF document expires 31 October 2026, so a purchasing file relying on it should request the current applicable copy.
Distinguish registration from approval
The FDA document is third-party verification of facility registration. FDA explains that it does not issue or recognize private registration certificates. A manufacturing-site GMP certificate is also distinct from a product-specific certification. Keep those distinctions in the supplier record without losing sight of the useful holder, scope and date information. FDA registration information; NSF GMP certification overview.
Connect the COA to the sampled batch
Request product or material identity, batch, specification version, test date, laboratory, methods, units, limits and results. Ingredient and finished-product reports should be labeled clearly. For heavy metals, ask about the individual lead, cadmium, arsenic and mercury panel, reporting limits and the acceptance basis for the market and material.
Complete the supplier file
Add the approved formula, sample record, artwork and packaging specification, test-document request and release responsibilities. Use the downloadable certificate library and the COA guide to organize an evidence request for a specific SKU.
| Record | Question it answers |
|---|---|
| Manufacturing-site certificate | Which holder, site, production scope and stated dates? |
| Raw-material COA | Which sampled ingredient lot and specification? |
| Finished-product report | Which formula, manufactured batch and test results? |
| Packaging approval | Which retail configuration and artwork version? |
A document checklist without invented laboratory results
| Document or result | Fields to check | What it does not establish |
|---|---|---|
| Manufacturing-site certificate | Holder, site, standard, scope, issue/expiry dates and surveillance conditions. | Approval of every SKU or every intended destination. |
| Batch COA | Product/formula identity, batch, test names, units, methods/limits and results. | A universal guarantee for a different batch or formula. |
| Individual metal report | Lead, cadmium, arsenic and mercury results with appropriate units, methods and limits. | An actual result if a report is only a blank template. |
The MITEYO document library identifies Guangdong Come Health Biotechnology Co., Ltd. on the supplied manufacturing-site documents. The public NSF cGMP copy states an expiry of 31 October 2026. Confirm the current copy and relevant manufacturing scope for the order. This checklist describes fields to review; it is not a sample laboratory report and contains no invented passing values.