FDA-Inspected Site

DMG America LLC dba Goldsmith & Revere, Inc.

6 FDA inspections are on record for DMG America LLC dba Goldsmith & Revere, Inc. in Englewood, United States.

483· Form 483 issued

Englewood, United States · Last updated July 10, 2026

Overview

  • 6 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2015-11-12.

At a glance

Inspections

6

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
6 Nov 2015 – 12 Nov 2015Medical Devices & Rad Health483View 483 →
13 Nov 2013Medical Devices & Rad HealthClean
20 Mar 2012Not recorded483View 483 →
7 Jul 2010Not recordedClean
17 Jan 2006Not recordedClean
16 Oct 2002Not recordedClean

Observations on record

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

12 Nov 2015
21 CFR 820.198(c)

Investigation of device failures

Cited by Charles Chacko

12 Nov 2015
21 CFR 820.75(b)(2)

Documentation of validated process performance

Cited by Charles Chacko

20 Mar 2012
21 CFR 820.20(b)

Lack of or inadequate organizational structure

Cited by David H Smith

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 820.198(c)Cited across public-safe Form 483 observations1x
21 CFR 820.20(b)Cited across public-safe Form 483 observations1x
21 CFR 820.75(b)(2)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind DMG America LLC dba Goldsmith & Revere, Inc.'s 2 Form 483s

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