FDA Inspection 1017084 — Jeremy Burkholder
The FDA completed an inspection of Jeremy Burkholder on July 6, 2017 in Lebanon, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 6, 2017
- Fiscal Year
- 2017
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Lebanon, PA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1360 | FDCA 501(a)(5) | Expired drugs administered |
| 1362 | 21 CFR 530.11(a) | Species or class |
| 4093 | 21 CFR 530.11(d) | ELDU - producer causes Illegal drug residue |
| 4185 | FDCA 402(a)(4) | Record keeping |