FDA-Inspected Site

Greer Laboratories, Inc.

20 FDA inspections are on record for Greer Laboratories, Inc. in Lenoir, United States.

483· Form 483 issued

Lenoir, United States · Last updated August 15, 2026

Overview

  • 20 FDA inspections are on record.
  • 8 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-12-12.

At a glance

Inspections

20

Form 483s

8

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
3 Dec 2025 – 12 Dec 2025Human Drugs483View 483 →
10 Dec 2024 – 18 Dec 2024Biologics483View 483 →
25 Oct 2022 – 1 Nov 2022Medical Devices & Rad Health483View 483 →
4 Sep 2019 – 11 Sep 2019Biologics483View 483 →
15 Nov 2017 – 22 Nov 2017Biologics483On file
7 Jun 2017 – 15 Jun 2017Medical Devices & Rad Health483View 483 →
18 Aug 2015 – 27 Aug 2015Biologics483On file
11 Mar 2014 – 12 Mar 2014Medical Devices & Rad HealthClean
5 Nov 2013 – 15 Nov 2013Human DrugsWL
15 Feb 2012Not recordedClean
7 Dec 2011Not recordedClean
29 Jun 2010Not recordedClean

Observations on record

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

12 Dec 2025
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Santos E Camara, Samantha E Cleek, Mabany Lizardi

12 Dec 2025
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Santos E Camara, Samantha E Cleek, Mabany Lizardi

18 Dec 2024
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Peng Zhou, Laurel A Beer

18 Dec 2024
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Peng Zhou, Laurel A Beer

18 Dec 2024
21 CFR 211.42(c)(10)(iv)

Environmental Monitoring System

Cited by Peng Zhou, Laurel A Beer

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 820.100(a)Cited across public-safe Form 483 observations3x
21 CFR 820.22Cited across public-safe Form 483 observations3x
21 CFR 211.22(d)Cited across public-safe Form 483 observations2x
21 CFR 820.120(b)Cited across public-safe Form 483 observations2x
21 CFR 820.181Cited across public-safe Form 483 observations2x
21 CFR 820.184Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(d)Cited across public-safe Form 483 observations2x
21 CFR 111.120(c)Cited across public-safe Form 483 observations1x
21 CFR 123.8(a)(3)(ii)Cited across public-safe Form 483 observations1x
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(d)Cited across public-safe Form 483 observations1x
21 CFR 211.113(a)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(iv)Cited across public-safe Form 483 observations1x
21 CFR 211.58Cited across public-safe Form 483 observations1x
21 CFR 211.67(b)Cited across public-safe Form 483 observations1x
21 CFR 806.10(b)Cited across public-safe Form 483 observations1x
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(3)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Greer Laboratories, Inc.'s 8 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