FDA-Inspected Site

Smisson-Cartledge Biomedical, LLC

5 FDA inspections are on record for Smisson-Cartledge Biomedical, LLC in Macon, United States.

Clean· No action indicated

Macon, United States · Last updated August 15, 2026

Overview

  • 5 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2023-09-15.

At a glance

Inspections

5

Form 483s

2

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
11 Sep 2023 – 15 Sep 2023Medical Devices & Rad HealthClean
27 Feb 2018 – 28 Feb 2018Medical Devices & Rad HealthClean
5 May 2014 – 16 May 2014Medical Devices & Rad Health483View 483 →
15 Nov 2011Not recorded483On file
18 Sep 2009Not recordedClean

Observations on record

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

16 May 2014
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Dawn M Braswell

16 May 2014
21 CFR 820.184

DHR content

Cited by Dawn M Braswell

Investigators

FDA investigators tied to this site in the record.

Paul W Moy1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Smisson-Cartledge Biomedical, LLC's 2 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