FDA Warning Letter — Advanced Sterilization Products

Case 82084 — FEI 3003662624

The FDA took a Warning Letter action against Advanced Sterilization Products on March 12, 2010 (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
Advanced Sterilization Products
Date
March 12, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)