Quality and compliance
Intertek-assessed GMP and ISO 22716 cosmetics manufacturing system.
Compliance is written precisely: no false FDA-certified claims, no unsupported medical claims, and product documents only where applicable.
Quality proof stack
Separate factory-system trust from product-specific documents.
cosmetics manufacturing practice anchor
cosmetics GMP guideline standard
current certificate validity year
Intertek GMP Certificate
- Standard
- Cosmetic Good Manufacturing Practice Guidelines (2022) published by U.S. Food and Drug Administration
- Issuer
- Intertek Testing Services
- Certificate No.
- SZ2508E6
- Issue Date
- 2025-08-15
- Valid Until
- 2028-08-14
Intertek ISO 22716 Certificate
- Standard
- ISO 22716:2007 Cosmetics - Guidelines on Good Manufacturing Practices
- Issuer
- Intertek Testing Services
- Certificate No.
- SZ2508E5
- Issue Date
- 2025-08-15
- Valid Until
- 2028-08-14
B2B document support
Compliance documents should match the product and destination market.
King Metis keeps compliance wording precise. Factory system certificates support trust, while product-specific MSDS, COA, ingredient information, label details, and market documents depend on the final formula and order scope.
MSDS
Available where applicable after product details are confirmed.
COA
Available where applicable after product details are confirmed.
Ingredient information
Available where applicable after product details are confirmed.
Packaging information
Available where applicable after product details are confirmed.
Operational gates
A buyer-facing quality path from brief to documents.
Gate 1
Requirement confirmation
Clarify formula direction, packaging material, capacity, label language, destination market and expected document scope.
Gate 2
Sample review
Review texture, fragrance, color, appearance, packaging fit and buyer feedback before final quotation planning.
Gate 3
Production checkpoints
Use manufacturing-system evidence, workshop images and order-specific requirements to coordinate production expectations.
Gate 4
Document preparation
Prepare product-specific MSDS, COA or related documents where applicable after final formula and order details are confirmed.
Does King Metis provide product-specific MSDS and COA?
Product-specific MSDS, COA, and related documents can be prepared where applicable after formula, sample, and order details are confirmed.
Are GMP and ISO 22716 the same as market approval?
No. GMP and ISO 22716 describe manufacturing system assessment. Product registration, import, and labeling requirements depend on the destination market.