FDA Inspection 884202 — Carefusion Corporation

Carefusion Corporation — FEI 1625685

The FDA completed an inspection of Carefusion Corporation on June 20, 2014 in Mannford, OK. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 20, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mannford, OK (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints