FDA Inspection 1088089 — Glick, Amos
The FDA completed an inspection of Glick, Amos on May 1, 2019 in Drumore, PA. 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
- May 1, 2019
- Fiscal Year
- 2019
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Drumore, PA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 4093 | 21 CFR 530.11(d) | ELDU - producer causes Illegal drug residue |
| 4182 | FDCA 501(a)(5) | ELDU without veterinary client-patient relationship |
| 4185 | FDCA 402(a)(4) | Record keeping |
| 4186 | FDCA 402(a)(4) | System for administration of drugs |
| 7001 | FDCA 402(a)(4) | Drug inventory (control of drugs on premises) |