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Eurofins Lancaster Laboratories, LLC

FDA Regulatory Profile

Eurofins Lancaster Laboratories, LLC has 0 FDA recalls, 21 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 23, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections21Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 23, 2025Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Aug 26, 2025Lancaster, PADrugsVoluntary Action Indicated (VAI)2513291
May 30, 2025Portage, MIDrugsVoluntary Action Indicated (VAI)1833335
Dec 10, 2021Portage, MIDrugsNo Action Indicated (NAI)1833335
Oct 21, 2021Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Oct 17, 2019Lancaster, PAVeterinaryNo Action Indicated (NAI)2513291
Sep 13, 2019Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Jan 23, 2019Portage, MIDrugsNo Action Indicated (NAI)1833335
Feb 23, 2018Portage, MIDrugsNo Action Indicated (NAI)1833335
Sep 28, 2017Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Nov 4, 2016Portage, MIVeterinaryNo Action Indicated (NAI)1833335
Jun 19, 2015Lancaster, PADrugsNo Action Indicated (NAI)2513291
Aug 1, 2014Portage, MIDrugsVoluntary Action Indicated (VAI)1833335
Apr 14, 2014Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Jun 27, 2013Lancaster, PAVeterinaryNo Action Indicated (NAI)2513291
May 17, 2012Lancaster, PADrugsNo Action Indicated (NAI)2513291
Apr 25, 2012Portage, MIVeterinaryNo Action Indicated (NAI)1833335
May 6, 2011Portage, MIDrugsNo Action Indicated (NAI)1833335
Jan 25, 2011Lancaster, PABiologicsNo Action Indicated (NAI)2513291
Sep 7, 2010Lancaster, PADrugsVoluntary Action Indicated (VAI)2513291

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 2513291Lancaster, PA13Sep 23, 2025
FEI 1833335Portage, MI8May 30, 2025

FDA data resources

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