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FDA Inspection 1075139 — Fresenius Kabi USA LLC

Fresenius Kabi USA LLC — FEI 1450022

The FDA completed an inspection of Fresenius Kabi USA LLC on December 3, 2018 in Melrose Park, 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
December 3, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Melrose Park, IL (United States)

Facility

Other inspections at this facility

  • 1216183 (VAI Thu Aug 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1174894 (OAI Thu Jun 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1123748 (OAI Mon May 18 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943126 (NAI Fri Sep 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943391 (VAI Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources