FDA Inspection 1121881 — Hospira, Inc.

Hospira, Inc. — FEI 3004591926

The FDA completed an inspection of Hospira, Inc. on February 27, 2020 in Lake Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 27, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lake Forest, IL (United States)