FDA Inspection 658621 — Eurofins BioPharma Product Testing Columbia, LLC
The FDA completed an inspection of Eurofins BioPharma Product Testing Columbia, LLC on Apr 23, 2010 in Columbia, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 23, 2010
- Fiscal Year
- 2010
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Columbia, MO (United States)