FDA Inspection 1026836 — Otoki Corporation Daepoong Factory
The FDA completed an inspection of Otoki Corporation Daepoong Factory on Sep 18, 2017 in Umseong. 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). 6 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 18, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Umseong (Korea (the Republic of))
Citations
| ID | CFR | Description |
|---|---|---|
| 1316 | 21 CFR 113.87(c) | Initial temperature of container contents |
| 1330 | 21 CFR 113.100(a) | Process records - forms missing information |
| 1643 | 21 CFR 113.100(e) | Incomplete information |
| 2887 | 21 CFR 113.40(j) | Processing: conform to other systems |
| 3874 | 21 CFR 113.60(b) | Cooling water - not chlorinated, sanitized |
| 3877 | 21 CFR 113.60(c) | Coding - required elements |