FDA Inspection 1068252 — Cellpack Ag
The FDA completed an inspection of Cellpack Ag on September 20, 2018 in Villmergen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Villmergen (Switzerland)