FDA Inspection 629336 — Allpack Group AG
The FDA completed an inspection of Allpack Group AG on November 6, 2009 in Reinach BL. 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
- November 6, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Reinach BL (Switzerland)