FDA Warning Letter — KMI IMI Group
The FDA took a Warning Letter action against KMI IMI Group on March 19, 2013 (Irvine, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- KMI IMI Group
- Date
- March 19, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Irvine, CA (United States)