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FDA Inspection 674214 — Carefusion Corporation

Carefusion Corporation — FEI 1625685

The FDA completed an inspection of Carefusion Corporation on July 30, 2010 in Mannford, OK. 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
July 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Mannford, OK (United States)

Facility

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FDA data resources