FDA Inspection 1067732 — EUROAPI FRANCE
The FDA completed an inspection of EUROAPI FRANCE on Nov 17, 2017 in Vertolaye. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 17, 2017
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Vertolaye (France)
Additional details
Mutual Recognition Agreement (MRA)