FDA Warning Letter — Teco Diagnostics, Inc.

Case 113248 — FEI 1832216

The FDA took a Warning Letter action against Teco Diagnostics, Inc. on August 20, 2010 (Anaheim, 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
Teco Diagnostics, Inc.
Date
August 20, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Anaheim, CA (United States)