FDA Inspection 1241064 — Hospira, Inc.

Hospira, Inc. — FEI 3004591926

The FDA completed an inspection of Hospira, Inc. on June 7, 2024 in Lake Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 7, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lake Forest, IL (United States)