FDA Inspection 773742 — Fresenius USA Manufacturing, Inc.

Fresenius USA Manufacturing, Inc. — FEI 1713747

The FDA completed an inspection of Fresenius USA Manufacturing, Inc. on Mar 8, 2012 in Ogden, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 8, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ogden, UT (United States)

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