FDA inspection

Abbott Laboratories: FDA inspection ending Aug 24, 2012

FDA inspection 796961 · Voluntary Action Indicated (VAI) · North Chicago, IL

Key facts

Inspection ID 796961
Firm Abbott Laboratories
FEI number 1451914
Address Us Route 41, Martin Luther King Dr.
City North Chicago
State IL
ZIP 60064
Country United States
Fiscal year 2012
Inspection end date Aug 24, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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