FDA Inspection 1059654 — Tjoapack Netherlands BV
The FDA completed an inspection of Tjoapack Netherlands BV on May 25, 2018 in Etten-Leur. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 25, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Etten-Leur (Netherlands)