FDA Warning Letter — Fresenius USA Manufacturing, Inc.

Case 393723 — FEI 1713747

The FDA took a Warning Letter action against Fresenius USA Manufacturing, Inc. on Mar 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
Mar 5, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Ogden, UT (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.