FDA Inspection 841999 — Eurofins BioPharma Product Testing Hamburg GmbH
The FDA completed an inspection of Eurofins BioPharma Product Testing Hamburg GmbH on July 10, 2013 in Hamburg. 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
- July 10, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Hamburg (Germany)