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Labcorp Early Development Laboratories, Inc.

FDA Regulatory Profile

Labcorp Early Development Laboratories, Inc. has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 25, 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
Inspections18Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 25, 2025Greenfield, INDrugsVoluntary Action Indicated (VAI)1850039
Mar 9, 2022York, United KingdomDrugsVoluntary Action Indicated (VAI)3014911955
Mar 9, 2022Harrogate, United KingdomDrugsVoluntary Action Indicated (VAI)3002806712
Feb 14, 2020Madison, WIDrugsNo Action Indicated (NAI)2128592
Nov 21, 2019Greenfield, INDrugsNo Action Indicated (NAI)1850039
Sep 27, 2019Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Feb 8, 2019Chantilly, VADrugsNo Action Indicated (NAI)3004567108
Aug 24, 2018Madison, WIDrugsVoluntary Action Indicated (VAI)2128592
Jun 15, 2017Harrogate, United KingdomDrugsVoluntary Action Indicated (VAI)3002806712
Jan 20, 2016Greenfield, INDrugsNo Action Indicated (NAI)1850039
Jul 14, 2014Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Feb 22, 2013Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Nov 28, 2012Madison, WIVeterinaryNo Action Indicated (NAI)2128592
Sep 12, 2012Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Aug 23, 2011Madison, WIDrugsNo Action Indicated (NAI)2128592
Jul 15, 2011Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Jun 5, 2009Harrogate, United KingdomDrugsNo Action Indicated (NAI)3002806712
Mar 30, 2009Madison, WIDrugsNo Action Indicated (NAI)2128592

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 1850039Greenfield, IN3Jul 25, 2025
FEI 3002806712Harrogate, United Kingdom8Mar 9, 2022
FEI 3014911955York, United Kingdom1Mar 9, 2022
FEI 2128592Madison, WI5Feb 14, 2020
FEI 3004567108Chantilly, VA1Feb 8, 2019

FDA data resources

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