FDA Inspection 1124187 — Fresenius USA Manufacturing, Inc

Fresenius USA Manufacturing, Inc — FEI 3013546115

The FDA completed an inspection of Fresenius USA Manufacturing, Inc on Jun 26, 2020 in Knoxville, TN. 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
Jun 26, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Knoxville, TN (United States)

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