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FDA Inspection 987844 — CareFusion 303, Inc.

CareFusion 303, Inc. — FEI 2016493

The FDA completed an inspection of CareFusion 303, Inc. on September 30, 2016 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 30, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

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  • 1123377 (OAI Mon Apr 06 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1064813 (OAI Thu Sep 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 893045 (OAI Mon Sep 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources