FDA Inspection 674214 — Carefusion Corporation

Carefusion Corporation — FEI 1625685

The FDA completed an inspection of Carefusion Corporation on Jul 30, 2010 in Mannford, OK. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Mannford, OK (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.