FDA inspection

Hospira, Inc.: FDA inspection ending Apr 29, 2009

FDA inspection 584062 · Voluntary Action Indicated (VAI) · Clayton, NC

Key facts

Inspection ID 584062
Firm Hospira, Inc.
FEI number 1048698
Address 8484 US 70 Bus Hwy W
City Clayton
State NC
ZIP 27520
Country United States
Fiscal year 2009
Inspection end date Apr 29, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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