FDA Inspection 917473 — Eurofins BioPharma Product Testing Columbia, LLC
The FDA completed an inspection of Eurofins BioPharma Product Testing Columbia, LLC on Mar 6, 2015 in Columbia, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 6, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Columbia, MO (United States)