FDA inspection

Abbott Laboratories Inc. (St Jude Medical): FDA inspection ending Jul 27, 2017

FDA inspection 1034622 · Voluntary Action Indicated (VAI) · Saint Paul, MN

Key facts

Inspection ID 1034622
Firm Abbott Laboratories Inc. (St Jude Medical)
FEI number 1000139754
Address One St. Jude Medical Drive
City Saint Paul
State MN
ZIP 55117
Fiscal year 2017
Inspection end date Jul 27, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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