FDA Inspection 698666 — K.W. Griffen Company
The FDA completed an inspection of K.W. Griffen Company on November 18, 2010 in Norwalk, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 18, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- 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 |