FDA Inspection 1329820 — Tjoapack Netherlands BV
The FDA completed an inspection of Tjoapack Netherlands BV on Feb 13, 2025 in Etten-Leur. 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
- Feb 13, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Etten-Leur (Netherlands)
Additional Details
Mutual Recognition Agreement (MRA)