FDA Inspection 1126818 — Fresenius USA Manufacturing, Inc.

Fresenius USA Manufacturing, Inc. — FEI 1713747

The FDA completed an inspection of Fresenius USA Manufacturing, Inc. on Aug 13, 2020 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
Aug 13, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ogden, UT (United States)

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