FDA Inspection 791170 — Eurofins BioPharma Product Testing Columbia, LLC
The FDA completed an inspection of Eurofins BioPharma Product Testing Columbia, LLC on Jul 18, 2012 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
- Jul 18, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Columbia, MO (United States)