FDA Inspection 895118 — Eurofins Biopharma Product Testing Munich GmbH
The FDA completed an inspection of Eurofins Biopharma Product Testing Munich GmbH on September 12, 2014 in Planegg. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 12, 2014
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Planegg (Germany)