FDA Warning Letter — Generic Medical Devices, Inc.

Case 151734 — FEI 3006142121

The FDA took a Warning Letter action against Generic Medical Devices, Inc. on April 28, 2011 (Gig Harbor, WA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Generic Medical Devices, Inc.
Date
April 28, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Gig Harbor, WA (United States)