FDA inspection

Hospira, Inc.: FDA inspection ending Sep 24, 2015

FDA inspection 942202 · Voluntary Action Indicated (VAI) · Rocky Mount, NC

Key facts

Inspection ID 942202
Firm Hospira, Inc.
FEI number 1021343
Address Highway 301 North
City Rocky Mount
State NC
ZIP 27801
Country United States
Fiscal year 2015
Inspection end date Sep 24, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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