FDA Inspection 1065808 — Astrea Fontaine
The FDA completed an inspection of Astrea Fontaine on Nov 10, 2017 in Fontaine Les Dijon. 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 10, 2017
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Fontaine Les Dijon (France)
Additional details
Mutual Recognition Agreement (MRA)