FDA Warning Letter — Fresenius USA Manufacturing, Inc.

Case 393723 — FEI 1713747

The FDA took a Warning Letter action against Fresenius USA Manufacturing, Inc. on March 5, 2013 (Ogden, UT). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Fresenius USA Manufacturing, Inc.
Date
March 5, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Ogden, UT (United States)