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FDA Inspection 919007 — Hospira, Inc.

Hospira, Inc. — FEI 1925262

The FDA completed an inspection of Hospira, Inc. on April 3, 2015 in Mcpherson, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 3, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Mcpherson, KS (United States)

Facility

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Recent compliance actions

FDA data resources