FDA Inspection 750674 — ARxIUM Inc.
The FDA completed an inspection of ARxIUM Inc. on September 22, 2011 in Winnipeg. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- September 22, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Winnipeg (Canada)