FDA Warning Letter — Gibson Laboratories, LLC

Case 82745 — FEI 1050138

The FDA took a Warning Letter action against Gibson Laboratories, LLC on November 3, 2009 (Lexington, KY). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Gibson Laboratories, LLC
Date
November 3, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Lexington, KY (United States)