FDA Inspection 654478 — The Garmon Corporation
The FDA completed an inspection of The Garmon Corporation on April 5, 2010 in Temecula, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 5, 2010
- Fiscal Year
- 2010
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Temecula, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1926 | 21 CFR 211.166(b) | Adequate number of batches on stability |
| 1942 | 21 CFR 211.180(e) | Records reviewed annually |
| 3553 | 21 CFR 211.48(a) | Plumbing System Defects |
| 3555 | 21 CFR 211.48(b) | Drains--Size, Back-siphonage Prevention |
| 4132 | 21 CFR 589.2000(d)(1) | Protein blenders, feed manufacturers, distributors |