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FDA Inspection 1078836 — Carefusion 2200 Inc

Carefusion 2200 Inc — FEI 3008002452

The FDA completed an inspection of Carefusion 2200 Inc on November 15, 2018 in Vernon Hills, 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
November 15, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Vernon Hills, IL (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1181731 (VAI Wed Oct 19 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 926924 (VAI Thu May 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855080 (OAI Tue Nov 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 743357 (VAI Wed Sep 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources