FDA Warning Letter — Steritec Products Mfg. Co., Inc.
The FDA took a Warning Letter action against Steritec Products Mfg. Co., Inc. on Oct 17, 2008 (Englewood, CO). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Steritec Products Mfg. Co., Inc.
- Date
- Oct 17, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Center
- CDRH
- Location
- Englewood, CO (United States)