FDA-Inspected Site

Gardner Denver Thomas Inc

2 FDA inspections are on record for Gardner Denver Thomas Inc in Monroe, United States.

483· Form 483 issued

Monroe, United States · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2015-02-06.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
5 Feb 2015 – 6 Feb 2015Medical Devices & Rad Health483View 483 →
3 Aug 2011Not recordedClean

Observations on record

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

6 Feb 2015
21 CFR 806.20(b)(4)

Justification for not reporting

Cited by Francis A Guidry

6 Feb 2015
21 CFR 820.72(b)

Calibration procedures - content

Cited by Francis A Guidry

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 806.20(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 820.72(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Gardner Denver Thomas Inc'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