FDA Warning Letter — Lone Star Medical Products, Inc.

Case 362439 — FEI 1627186

The FDA took a Warning Letter action against Lone Star Medical Products, Inc. on April 25, 2013 (Stafford, TX). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Lone Star Medical Products, Inc.
Date
April 25, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Stafford, TX (United States)