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FDA Inspection 812876 — Fresenius Kabi Warrendale

Fresenius Kabi Warrendale — FEI 3005778453

The FDA completed an inspection of Fresenius Kabi Warrendale on December 20, 2012 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
December 20, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Warrendale, PA (United States)

Facility

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FDA data resources