FDA Inspection 829858 — Continental Vitamin Company Inc
The FDA completed an inspection of Continental Vitamin Company Inc on Apr 2, 2013 in Vernon, 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: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 2, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Vernon, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1133 | 21 CFR 211.25(a) | GMP Training Frequency |
| 3559 | 21 CFR 211.56(a) | Sanitation--buildings not clean, free of infestation |
| 3629 | 21 CFR 211.170(b) | Reserve samples identified, representative, stored |
| 4391 | 21 CFR 211.180(e)(2) | Items to cover on annual reviews |