FDA-Inspected Site

Medtronic Inc.

3 FDA inspections are on record for Medtronic Inc. in Minneapolis, United States.

Clean· No action indicated

Minneapolis, United States · Last updated July 10, 2026

Overview

  • 3 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-11-13.

At a glance

Inspections

3

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
13 Nov 2017Medical Devices & Rad HealthClean
8 Dec 2011Not recordedClean
22 Oct 2010Not recorded483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

22 Oct 2010
21 CFR 812.35(a)(1)

No approval for changes requiring prior approval

Cited by Aimee J Edwin

Investigators

FDA investigators tied to this site in the record.

MDSAP WilliamsA1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 812.35(a)(1)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Medtronic Inc.'s 1 Form 483

Verbatim observations and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat