FDA Inspection 605503 — Cardinal Health

Cardinal Health — FEI 3007123846

The FDA completed an inspection of Cardinal Health on Aug 19, 2009 in Olathe, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 19, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Olathe, KS (United States)