FDA Inspection 1320892 — Curium Netherlands B.V.
The FDA completed an inspection of Curium Netherlands B.V. on May 17, 2024 in Petten. 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
- May 17, 2024
- Fiscal Year
- 2024
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Petten (Netherlands)
Additional details
Mutual Recognition Agreement (MRA)