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FDA Inspection 1030393 — Fresenius Kabi Warrendale

Fresenius Kabi Warrendale — FEI 3005778453

The FDA completed an inspection of Fresenius Kabi Warrendale on September 14, 2017 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
September 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Warrendale, PA (United States)

Facility

Other inspections at this facility

  • 1237140 (NAI Tue Apr 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924837 (NAI Tue May 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 812876 (NAI Thu Dec 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 735611 (NAI Fri May 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 541136 (NAI Tue Oct 07 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources