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Certifications资质认证

Three credential records you can look up: ISO 9001:2015 (749435), CGMP-ASEAN (912/GCN-QLD, Drug Administration of Vietnam), and US FDA facility registration (FEI 3030839348 — a filing under MoCRA, not an approval or a certification). Numbers are listed here.

Three credential records 3

ISO 9001:2015
Cert. no. 749435
Issued by Guardian Independent Certification (UK, UKAS 045)
Scope: manufacture and trade of wet cosmetics
Issued 2024-08-20 · Valid to 2027-08-17
CGMP-ASEAN
No. 912/GCN-QLD
Drug Administration of Vietnam
Issued 2023-12-06 · Renewal in progress
US FDA
Facility registration · FEI 3030839348
Registered 2024-05 to 2026-05 · expired 2026-05-31
A filing under MoCRA — not an approval or certification

What each one does and does not prove

ISO 9001:2015 is a quality management system certificate, issued by Guardian Independent Certification (UK, UKAS 045), and the scope printed on it reads "manufacture and trade of wet cosmetics". It shows the plant runs to the standard; it is not a pass mark for any individual product. UKAS 045 is the UK accreditation number, so the issuer can be checked separately.

CGMP-ASEAN is Good Manufacturing Practice issued by the Drug Administration of Vietnam, no. 912/GCN-QLD, issued 2023-12-06. Renewal is in progress.

US FDA is worth reading literally: it is a facility registration, not an approval and not a certification. FEI 3030839348, registration completed 2024-05 to 2026-05 under MoCRA — that window expired on 2026-05-31 and renewal has not been confirmed. It grants no product access to the US market.

Why the certificates show a Long An address

On the address printed on the certificates: it keeps the Long An wording. It is the same site as Tay Ninh Province listed on this site — provincial boundaries were redrawn in 2025 and the certificates are not re-issued before expiry.

How to verify these numbers

Every number can be looked up. If you need the original of one of these, tell us the purpose and we arrange a review during evaluation. Scans are not published online, so they cannot be reused.

Market by market: compliance questions 6 Q&A

Do you hold ISO 22716 (cosmetics GMP)?
No. What we hold is CGMP-ASEAN (912/GCN-QLD, issued by the Drug Administration of Vietnam). They are not the same standard and one does not stand in for the other. If your market requires ISO 22716 specifically, we say we cannot meet it.
Do you hold HALAL certification?
No, we do not hold it. We turn down any order that requires halal certification. Indonesia is one market where that certification is mandatory.
For the EU, who handles CPNP and CPSR?
Both attach to the product and to the EU-based responsible person, not to the factory. CPNP is a notification database filed product by product; a CPSR is a safety report per product. Both must be filed by the responsible entity inside the EU. We do not handle either, and we cannot file under the factory name — the split is set out under "Who files the product registration" on the documents page.
Does the US FDA registration work as a product authorisation?
No. FEI 3030839348 is a facility registration, a filing under MoCRA. It is neither an approval nor a certification and it grants no product access to the US market.
Can you issue a certificate of origin? What are CTC and LVC?
Yes, issued to the destination requirement. CTC is change of tariff classification; LVC is local value content. They are origin tests under different agreements. Which one applies and whether a shipment qualifies is checked tariff line by tariff line against the HS code, and we give the answer with the quote.
Can you simply send the certificate scans?
A review can be arranged during evaluation, with the purpose stated. We do not publish scans, so they cannot be reused.
Need the original of one of these? Tell us the purpose and we arrange a review.
Three lines, and the first reply can answer you
  1. CategoryWhich category, or simply "like that product of yours" — more useful than a formula name
  2. VolumeRoughly how many units or kilograms, per SKU
  3. MarketThe destination decides access and labelling — one formula going to the EU and to the US is not one set of documents
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