Charles River Laboratories Germany GmbH

FDA Regulatory Profile

Charles River Laboratories Germany GmbH has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 20, 2025 · VAI

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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
Inspections5Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 20, 2025Erkrath, GermanyDrugsVoluntary Action Indicated (VAI)3004512725
Aug 24, 2021Erkrath, GermanyDrugsVoluntary Action Indicated (VAI)3004512725
Dec 15, 2017Erkrath, GermanyDrugsVoluntary Action Indicated (VAI)3004512725
Mar 4, 2015Erkrath, GermanyDrugsNo Action Indicated (NAI)3004512725
Sep 23, 2011Erkrath, GermanyDrugsVoluntary Action Indicated (VAI)3004512725

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 3004512725Erkrath, Germany5Aug 20, 2025

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