FDA Inspection 1004486 — Keith L. Miller
The FDA completed an inspection of Keith L. Miller on Dec 22, 2016 in Newburgh, ME. 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). 5 citations were issued during this inspection. Product area: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 22, 2016
- Fiscal Year
- 2017
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Newburgh, ME (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1360 | FDCA 501(a)(5) | Expired drugs administered |
| 1366 | 21 CFR 530.11(a) | Dosage level |
| 4093 | 21 CFR 530.11(d) | ELDU - producer causes Illegal drug residue |
| 4185 | FDCA 402(a)(4) | Record keeping |
| 7001 | FDCA 402(a)(4) | Drug inventory (control of drugs on premises) |