FDA Inspection 698666 — K.W. Griffen Company
The FDA completed an inspection of K.W. Griffen Company on Nov 18, 2010 in Norwalk, CT. 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
- Nov 18, 2010
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Norwalk, CT (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 4314 | 21 CFR 211.84(d)(2) | Reports of Analysis (Components) |
| 4355 | 21 CFR 211.165(c) | Sampling and testing plans not followed |
| 4402 | 21 CFR 211.192 | Written record of investigation incomplete |