FDA Inspection 825720 — ARxIUM Inc.
The FDA completed an inspection of ARxIUM Inc. on March 27, 2013 in Winnipeg. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- March 27, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Winnipeg (Canada)