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FDA Inspection 893045 — CareFusion 303, Inc.

CareFusion 303, Inc. — FEI 2016493

The FDA completed an inspection of CareFusion 303, Inc. on September 29, 2014 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 29, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Facility

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Recent compliance actions

FDA data resources