FDA Inspection 1260879 — NIHON YAKKEN NORTH AMERICA, INC.
The FDA completed an inspection of NIHON YAKKEN NORTH AMERICA, INC. on Feb 13, 2025 in Marina Del Rey, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Feb 13, 2025
- Fiscal Year
- 2025
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Marina Del Rey, CA (United States)
Additional Details
FSVP
Citations
| ID | CFR | Description |
|---|---|---|
| 18254 | 21 CFR 1.502(a) | Develop FSVP |
| 18263 | 21 CFR 1.504(b)(1) | Hazard analysis biological, chemical, physical |
| 18294 | 21 CFR 1.506(c) | Supplier verification assurance |
| 18303 | 21 CFR 1.506(e)(1) | Verification activity before import, periodically |