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Charles River Laboratories Edinburgh Ltd.

FDA Regulatory Profile

Charles River Laboratories Edinburgh Ltd. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 11, 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
Inspections8Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 11, 2026Tranent, United KingdomDrugsNo Action Indicated (NAI)1000544053
Sep 2, 2025Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Mar 8, 2024Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Nov 21, 2019Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Nov 10, 2016Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Dec 17, 2014Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Sep 12, 2012Tranent, United KingdomDrugsVoluntary Action Indicated (VAI)1000544053
Mar 2, 2009Tranent, United KingdomDrugsNo Action Indicated (NAI)1000544053

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 1000544053Tranent, United Kingdom8Jun 11, 2026

FDA data resources

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