FDA Inspection 1029902 — Continental Vitamin Company Inc
The FDA completed an inspection of Continental Vitamin Company Inc on Oct 26, 2017 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). 3 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 26, 2017
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Vernon, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1033 | 21 CFR 211.22(a) | Authority lacking to review records, investigate errors |
| 1274 | 21 CFR 211.68(a) | Calibration/Inspection/Checking not done |
| 4391 | 21 CFR 211.180(e)(2) | Items to cover on annual reviews |