FDA Inspection 1278254 — Hospira, Inc.

Hospira, Inc. — FEI 3004591926

The FDA completed an inspection of Hospira, Inc. on Aug 22, 2025 in Lake Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 22, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lake Forest, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.