FDA-Inspected Site

Charles River Laboratories, Inc.

10 FDA inspections are on record for Charles River Laboratories, Inc. in Charleston, United States.

483· Form 483 issued

Charleston, United States · Last updated July 10, 2026

Overview

  • 10 FDA inspections are on record.
  • 5 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-03-27.

At a glance

Inspections

10

Form 483s

5

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
23 Mar 2026 – 27 Mar 2026Human Drugs483View 483 →
15 Aug 2019 – 20 Aug 2019Human DrugsClean
13 May 2019 – 17 May 2019Biologics483On file
4 Jan 2016 – 13 Jan 2016Biologics483On file
21 Apr 2014 – 24 Apr 2014Human DrugsClean
15 Jan 2013Not recorded483On file
31 Mar 2009Not recorded483On file
20 Jan 2006Not recordedClean
13 Dec 2002Not recordedClean
9 May 2000Not recordedClean

Observations on record

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

27 Mar 2026
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Jennifer Lalama, Michael Z Weigman

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 211.22(d)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Charles River Laboratories, Inc.'s 5 Form 483s

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