FDA Inspection 1243871 — Greenland Inc
The FDA completed an inspection of Greenland Inc on Jul 11, 2024 in Seattle, WA. 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). 10 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 11, 2024
- Fiscal Year
- 2024
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Seattle, WA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1529 | 21 CFR 113.89 | Process deviation log/file |
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15584 | 21 CFR 111.155(d)(1) | Components - identify lot produced |
| 15761 | 21 CFR 111.205(b)(1) | Master manufacturing record - specifications; quality |
| 15829 | 21 CFR 111.70(b)(1) | Specifications - component identity |
| 15830 | 21 CFR 111.70(b)(2) | Specifications-component purity, strength, composition |
| 15832 | 21 CFR 111.70(c)(1) | In-process identity, purity, strength, composition |
| 15839 | 21 CFR 111.70(e) | Specifications - identity, purity, strength, composition |
| 15932 | 21 CFR 111.105(a) | Quality control - processes, specifications, written procedures |
| 3892 | 21 CFR 113.60(a) | Regular observations for gross closure defects |