FDA inspection

Medtronic Inc.: FDA inspection ending Nov 13, 2017

FDA inspection 1045908 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 1045908
Firm Medtronic Inc.
FEI number 3008114455
Address 3033 Campus Dr
City Minneapolis
State MN
ZIP 55441-2651
Fiscal year 2018
Inspection end date Nov 13, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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