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FDA Inspection 1019824 — Fresenius Kabi USA LLC

Fresenius Kabi USA LLC — FEI 3008604776

The FDA completed an inspection of Fresenius Kabi USA LLC on July 20, 2017 in Skokie, IL. 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
July 20, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Skokie, IL (United States)

Facility

Other inspections at this facility

  • 1123044 (NAI Thu Mar 05 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919270 (NAI Tue Mar 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 837141 (NAI Tue Jun 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 797104 (NAI Fri Sep 07 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710516 (NAI Thu Feb 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources