FDA-Inspected Site

Essex Industries, Inc.

6 FDA inspections are on record for Essex Industries, Inc. in Affton, United States.

483· Form 483 issued

Affton, United States · Last updated July 10, 2026

Overview

  • 6 FDA inspections are on record.
  • 4 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-02-23.

At a glance

Inspections

6

Form 483s

4

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
18 Feb 2026 – 23 Feb 2026Medical Devices & Rad Health483View 483 →
5 Dec 2022 – 16 Dec 2022Medical Devices & Rad Health483View 483 →
22 Mar 2016 – 23 Mar 2016Medical Devices & Rad HealthClean
8 Jul 2013 – 10 Jul 2013Medical Devices & Rad Health483View 483 →
15 Dec 2009Not recorded483On file
17 Jan 2001Not recordedClean

Observations on record

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

23 Feb 2026
21 CFR 830.300(a)

Devices subject to device identification GUDID data submission requirements.

Cited by Edward E Lockwood

23 Feb 2026
21 CFR 830.300(a)

Devices subject to device identification GUDID data submission requirements.

Cited by Edward E Lockwood

16 Dec 2022
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Mary L Schuckmann

16 Dec 2022
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Mary L Schuckmann

16 Dec 2022
21 CFR 820.198(c)

Investigation of device failures

Cited by Mary L Schuckmann

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
21 CFR 820.198(c)Cited across public-safe Form 483 observations2x
21 CFR 830.300(a)Cited across public-safe Form 483 observations2x
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Essex Industries, Inc.'s 4 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