FDA Inspection 770775 — Cardinal Health

Cardinal Health — FEI 3007123846

The FDA completed an inspection of Cardinal Health on Mar 1, 2012 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
Mar 1, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Olathe, KS (United States)