FDA-Inspected Site

Covidien, LP

7 FDA inspections are on record for Covidien, LP in Norfolk, United States.

483· Form 483 issued

Norfolk, United States · Last updated July 9, 2026

Overview

  • 7 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-11-15.

At a glance

Inspections

7

Form 483s

1

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
13 Nov 2017 – 15 Nov 2017Medical Devices & Rad Health483View 483 →
21 Mar 2016 – 23 Mar 2016Medical Devices & Rad HealthClean
14 Apr 2015 – 17 Apr 2015Medical Devices & Rad HealthClean
15 Dec 2011Not recordedClean
19 Nov 2008Not recordedClean
31 Jan 2008Not recordedClean
15 Dec 2000Not recordedClean

Observations on record

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

15 Nov 2017
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Eric C Fox, Eric M Padgett

15 Nov 2017
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Eric C Fox, Eric M Padgett

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Covidien, LP's 1 Form 483

Source PDFs, 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