FDA Warning Letter — Aionex, Inc.
The FDA took a Warning Letter action against Aionex, Inc. on January 9, 2013 (Madison, TN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Aionex, Inc.
- Date
- January 9, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Madison, TN (United States)