FDA Inspection 906256 — Hospira, Inc.

Hospira, Inc. — FEI 3004591926

The FDA completed an inspection of Hospira, Inc. on December 9, 2014 in Lake Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 9, 2014
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Lake Forest, IL (United States)