FDA Inspection 1204381 — Tiofarma B.V.
The FDA completed an inspection of Tiofarma B.V. on Jul 6, 2021 in Oud-Beijerland. 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
- Jul 6, 2021
- Fiscal Year
- 2021
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Oud-Beijerland (Netherlands)
Additional details
Mutual Recognition Agreement (MRA)