FDA inspection

Hospira, Inc.: FDA inspection ending Sep 9, 2013

FDA inspection 846706 · No Action Indicated (NAI) · Lake Forest, IL

Key facts

Inspection ID 846706
Firm Hospira, Inc.
FEI number 3004591926
Address 375 N Field Dr
City Lake Forest
State IL
ZIP 60045
Country United States
Fiscal year 2013
Inspection end date Sep 9, 2013
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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