FDA Inspection 667733 — AEIOMed, Inc.
The FDA completed an inspection of AEIOMed, Inc. on Jun 3, 2010 in New Brighton, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 3, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Brighton, MN (United States)