FDA Inspection 1015295 — Fresenius USA Manufacturing, Inc.

Fresenius USA Manufacturing, Inc. — FEI 1713747

The FDA completed an inspection of Fresenius USA Manufacturing, Inc. on May 18, 2017 in Ogden, UT. 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
May 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Ogden, UT (United States)

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