FDA Warning Letter — Tricol Biomedical, Inc.

Case 420554 — FEI 3004050854

The FDA took a Warning Letter action against Tricol Biomedical, Inc. on May 20, 2014 (Portland, OR). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Tricol Biomedical, Inc.
Date
May 20, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Portland, OR (United States)