FDA-Inspected Site

Wm. E. Martin & Sons Co., Inc.

5 FDA inspections are on record for Wm. E. Martin & Sons Co., Inc. in Roslyn, United States.

483· Form 483 issued

Roslyn, United States · Last updated July 11, 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

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
31 Aug 2023 – 15 Sep 2023Foods & Cosmetics483On file
1 Aug 2011Not recorded483View 483 →
11 Mar 2010Not recordedClean
4 Feb 2010Not recordedClean
22 Aug 2003Not recordedClean

Observations on record

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

1 Aug 2011
21 CFR 110.80(b)(2)

Manufacturing conditions

Cited by Shreya Shah, Frank Verni

Investigators

FDA investigators tied to this site in the record.

Nicholas E Squillante1 insp.
Jane Chen1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 110.80(b)(2)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Wm. E. Martin & Sons Co., 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