FDA inspection

Hospira, Inc.: FDA inspection ending Jun 7, 2024

FDA inspection 1241064 · No Action Indicated (NAI) · Lake Forest, IL

Key facts

Inspection ID 1241064
Firm Hospira, Inc.
FEI number 3004591926
Address 375 N Field Dr
City Lake Forest
State IL
ZIP 60045
Country United States
Fiscal year 2024
Inspection end date Jun 7, 2024
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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