FDA Inspection 735611 — Fresenius Kabi Warrendale

Fresenius Kabi Warrendale — FEI 3005778453

The FDA completed an inspection of Fresenius Kabi Warrendale on May 27, 2011 in Warrendale, PA. 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
May 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Warrendale, PA (United States)