FDA Warning Letter — Steripac
The FDA took a Warning Letter action against Steripac on December 29, 2009 (Birmingham, AL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Steripac
- Date
- December 29, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Birmingham, AL (United States)