FDA Inspection 876340 — Hospira, Inc.

Hospira, Inc. — FEI 1925262

The FDA completed an inspection of Hospira, Inc. on April 23, 2014 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 23, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mcpherson, KS (United States)