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Charles River Laboratories, Inc.

FDA Regulatory Profile

Charles River Laboratories, Inc. has 0 FDA recalls, 28 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 1, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections28Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 1, 2026Saint-Laurent, CanadaDrugsNo Action Indicated (NAI)3043236302
Apr 2, 2026Wayne, PADrugsNo Action Indicated (NAI)3015687403
Mar 27, 2026Charleston, SCDrugsVoluntary Action Indicated (VAI)1053022
Jan 20, 2026Malvern, PADrugsNo Action Indicated (NAI)1000121235
Sep 17, 2025Shrewsbury, MADrugsNo Action Indicated (NAI)3006088423
Sep 9, 2025Wilmington, MADrugsVoluntary Action Indicated (VAI)1000086712
May 2, 2025Wilmington, MABiologicsNo Action Indicated (NAI)1000086712
Jan 4, 2024Malvern, PADrugsVoluntary Action Indicated (VAI)1000121235
Nov 9, 2022Wayne, PADrugsNo Action Indicated (NAI)3015687403
Oct 1, 2020Spencerville, OHDrugsVoluntary Action Indicated (VAI)1523647
Mar 19, 2020Wayne, PADrugsNo Action Indicated (NAI)3015687403
Feb 11, 2020Wilmington, MADrugsVoluntary Action Indicated (VAI)1000086712
Aug 20, 2019Charleston, SCDrugsNo Action Indicated (NAI)1053022
Jul 26, 2019Skokie, ILDrugsVoluntary Action Indicated (VAI)3007838011
May 17, 2019Charleston, SCBiologicsVoluntary Action Indicated (VAI)1053022
Jan 17, 2019Malvern, PADrugsNo Action Indicated (NAI)1000121235
Nov 9, 2018Shrewsbury, MADrugsNo Action Indicated (NAI)3006088423
Jun 21, 2017Wilmington, MADrugsVoluntary Action Indicated (VAI)1000086712
Dec 6, 2016Shrewsbury, MADrugsVoluntary Action Indicated (VAI)3006088423
Jan 13, 2016Charleston, SCBiologicsVoluntary Action Indicated (VAI)1053022

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3043236302Saint-Laurent, Canada1May 1, 2026
FEI 3015687403Wayne, PA3Apr 2, 2026
FEI 1053022Charleston, SC7Mar 27, 2026
FEI 1000121235Malvern, PA6Jan 20, 2026
FEI 3006088423Shrewsbury, MA4Sep 17, 2025
FEI 1000086712Wilmington, MA5Sep 9, 2025
FEI 1523647Spencerville, OH1Oct 1, 2020
FEI 3007838011Skokie, IL1Jul 26, 2019

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.