FDA Inspection 1091920 — Eurofins Pharma Quality Control
The FDA completed an inspection of Eurofins Pharma Quality Control on September 8, 2017 in Les Ulis. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 8, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Les Ulis (France)
Additional Details
Mutual Recognition Agreement (MRA)