FDA Inspection 667733 — AEIOMed, Inc.
The FDA completed an inspection of AEIOMed, Inc. on June 3, 2010 in New Brighton, MN. 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
- June 3, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Brighton, MN (United States)