FDA Warning Letter — Fresenius USA Manufacturing, Inc.

Case 730319 — FEI 1713747

The FDA took a Warning Letter action against Fresenius USA Manufacturing, Inc. on Aug 25, 2026 (Ogden, UT). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Fresenius USA Manufacturing, Inc.
Date
Aug 25, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Ogden, UT (United States)

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