FDA Warning Letter — Continental Medical Labs, Inc.

Case 393779 — FEI 2128604

The FDA took a Warning Letter action against Continental Medical Labs, Inc. on March 6, 2013 (Waterford, WI). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Continental Medical Labs, Inc.
Date
March 6, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Waterford, WI (United States)