FDA Inspection 1329104 — Delpharm Dijon
The FDA completed an inspection of Delpharm Dijon on Dec 13, 2024 in Quetigny. 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
- Dec 13, 2024
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Quetigny (France)
Additional Details
Mutual Recognition Agreement (MRA)