FDA Inspection 790327 — AEIOMed, Inc.
The FDA completed an inspection of AEIOMed, Inc. on Jul 11, 2012 in New Brighton, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 11, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Brighton, MN (United States)