FDA Inspection 1195086 — Fresenius USA Manufacturing, Inc

Fresenius USA Manufacturing, Inc — FEI 3013546115

The FDA completed an inspection of Fresenius USA Manufacturing, Inc on Dec 7, 2022 in Knoxville, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 7, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Knoxville, TN (United States)

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