Certification and audit

ISO 22716 certified, FDA-registered cosmetics manufacturing

SGS audited this Guangzhou factory to ISO 22716:2007 and to the US FDA cFSAN cosmetics GMP guidance in March 2026, both certificates valid to March 2029, and the facility holds a US FDA registration number. The scans, the exact production scope and the limits of each document are below.

ISO 22716:2007
SGS CN26/00001382 · valid to Mar 2029
US FDA cFSAN GMP
SGS CN26/00001379 · valid to Mar 2029
FDA facility registration
FEI 3041697230
Audited scope
Serums, creams, toners, gels, masks
Cleared for
Eye-area and infant cosmetics
SGS ISO 22716:2007 cosmetics GMP certificate CN26/00001382 issued to Guangzhou Jinchen Biotechnology Co., Ltd., valid to 4 March 2029

Complete certificate page, unedited. Issued by SGS in Chinese; the English transcription is beside it. Tap to open at full size.

SGS · ISO 22716:2007

ISO 22716:2007 — GMP certification for cosmetics manufacturing

Certificate no.
CN26/00001382
Standard
ISO 22716:2007 — Cosmetics, Good Manufacturing Practices
Issued to
Guangzhou Jinchen Biotechnology Co., Ltd.
Issued by
SGS Hong Kong Limited
Valid
5 March 2026 — 4 March 2029
Production scope
Production of cosmetics in the general liquid unit (hair cleansing, skin toners, gels) and in the cream and lotion unit (skin cleansing). The schedule carries the # suffix, which confirms the line is also cleared for eye-area products and for infant and child cosmetics.

What it certifies

An accredited third party has audited the workshop against the international cosmetics GMP standard. This is the certificate EU, UK and Gulf buyers ask for first, and it covers the same line that fills serums, creams and masks.

Scope and limits

It certifies the management system and the production scope listed on the schedule. It is not a product approval, and formulas outside that scope are not covered.

SGS certificate CN26/00001379 confirming US FDA cFSAN cosmetics GMP conformity for Guangzhou Jinchen Biotechnology Co., Ltd. factory

Complete certificate page, unedited. Issued by SGS in Chinese; the English transcription is beside it. Tap to open at full size.

SGS · US FDA cFSAN GMP

US FDA cFSAN cosmetics GMP — SGS certificate of conformity

Certificate no.
CN26/00001379
Standard
US FDA cFSAN Good Manufacturing Practice for cosmetics (2008)
Issued to
Guangzhou Jinchen Biotechnology Co., Ltd.
Issued by
SGS-CSTC Standards Technical Services Co., Ltd.
Valid
5 March 2026 — 4 March 2029
Production scope
The same production scope as the ISO 22716 certificate: general liquid unit and cream and lotion unit, with the # suffix covering eye-area products and infant and child cosmetics.

What it certifies

The workshop has been assessed against the US FDA guidance as well as the ISO standard, so a US buyer does not have to take the ISO certificate on trust alone.

Scope and limits

An SGS conformity certificate against FDA guidance. It is not issued by the FDA, and it is not an FDA approval of any product.

US FDA facility registration certificate, FEI 3041697230, cosmetic product facility under MoCRA, Golden Palace Biotechnology

Complete certificate page, unedited. Issued in English by the registering agent. Tap to open at full size.

TMC · US FDA facility registration

US FDA facility registration — cosmetic product facility under MoCRA

Certificate no.
FEI 3041697230
Standard
MoCRA facility registration (Cosmetic Modernization Act, 2022)
Issued to
Golden Palace Biotechnology Int’l Co., Ltd.
Issued by
TMC — US FDA registered agent
Valid
29 November 2025 — Renewed every two years under section 607(a)(2)
Production scope
Facility registration as a manufacturer of cosmetic products. Product listings are updated annually under section 607(c)(5).
Name on the document
Recorded under the company trading name, not the licence holder. The workshop address is the same one printed on the SGS certificates, and the FEI number belongs to that address — see "One factory, three names" below.

What it certifies

The facility holds a US FDA registration number, which a US importer needs before a cosmetic shipment can be cleared through customs.

Scope and limits

Registration only. Issued by the registered agent, not by the FDA, and not an approval or endorsement of any product.

Company identity

One factory, three names on the paperwork

The company sells under the Golden Palace name internationally. The manufacturing entity is the one named on the production licence. The FDA facility record carries the trading name. All three point at the same workshop, the same line and the same team — here is where each name appears.

  • Brand used on this siteGoldenPalaceThe name buyers see, quote and message us on.
  • Trading name on the FDA facility recordGolden Palace Biotechnology Int’l Co., Ltd.Recorded against FEI 3041697230. A trading name, not a separate registered company.
  • Manufacturing entity on the licenceGuangzhou Jinchen Biotechnology Co., Ltd.Holder of Guangdong cosmetics production licence 20190241 and the SGS certificates. This is the entity on your invoice and contract.

The workshop address printed on the FDA record — Building 11, 678 Guangcong North Road, Taiping Town, Conghua District, Guangzhou — is the same address carried by the SGS certificates and the production licence, and the FEI number is attached to that address. The audit behind the SGS certificates was carried out on the same production floor.

Your quotation, contract and shipping documents are issued by Guangzhou Jinchen Biotechnology Co., Ltd., so the entity you pay and the entity on the licence are one and the same. Ask before you commit and we will confirm in writing which name sits on which document.

Certificates are issued to Guangzhou Jinchen Biotechnology Co., Ltd. — Production Licence 20190241. A product-specific test report, SGS CANWT00476140, and the full-size scans are supplied with your quotation. To verify any certificate independently, quote its number to SGS or to the registering agent named above.

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