FDA-Inspected Site

Gendron Inc.

4 FDA inspections are on record for Gendron Inc. in Bryan, United States.

483· Form 483 issued

Bryan, United States · Last updated July 10, 2026

Overview

  • 4 FDA inspections are on record.
  • 3 inspections produced a Form 483.
  • The most recent recorded inspection date is 2018-03-16.

At a glance

Inspections

4

Form 483s

3

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
12 Mar 2018 – 16 Mar 2018Medical Devices & Rad Health483View 483 →
24 Jun 2014 – 2 Jul 2014Medical Devices & Rad Health483On file
11 Sep 2009Not recorded483View 483 →
28 Sep 2001Not recordedClean

Observations on record

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

16 Mar 2018
21 CFR 803.17

Lack of Written MDR Procedures

Cited by David J Gasparovich

16 Mar 2018
21 CFR 803.17

Lack of Written MDR Procedures

Cited by David J Gasparovich

16 Mar 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by David J Gasparovich

16 Mar 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by David J Gasparovich

16 Mar 2018
21 CFR 820.198(d)

Evaluation, timeliness, identification

Cited by David J Gasparovich

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 820.22Cited across public-safe Form 483 observations3x
21 CFR 803.17Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(d)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.40(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Gendron Inc.'s 3 Form 483s

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