FDA Inspection 667215 — Fresenius U.S.A. Manufacturing

Fresenius U.S.A. Manufacturing — FEI 1527681

The FDA completed an inspection of Fresenius U.S.A. Manufacturing on June 15, 2010 in Oregon, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 15, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Oregon, OH (United States)