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UPS Supply Chain Solutions, Inc.

FDA Regulatory Profile

UPS Supply Chain Solutions, Inc. has 0 FDA recalls, 22 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 30, 2025 · 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
Inspections22Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 30, 2025Fairdale, KYFood/CosmeticsNo Action Indicated (NAI)3019946577
Jul 24, 2023Louisville, KYDevicesNo Action Indicated (NAI)3006759904
Jul 21, 2023Louisville, KYDevicesNo Action Indicated (NAI)3006759904
Jul 20, 2023Louisville, KYDevicesNo Action Indicated (NAI)3006759904
Jun 29, 2023Durham, NCDrugsNo Action Indicated (NAI)3014367401
Sep 12, 2022Louisville, KYBiologicsNo Action Indicated (NAI)3006759904
Jan 22, 2020Malden, MADevicesNo Action Indicated (NAI)3004927096
Aug 15, 2019Louisville, KYBiologicsNo Action Indicated (NAI)3006759904
Sep 21, 2018Harrisburg, PAFood/CosmeticsNo Action Indicated (NAI)3004695776
Sep 29, 2016Harrisburg, PAFood/CosmeticsNo Action Indicated (NAI)3004695776
Jun 15, 2016Eastvale, CAFood/CosmeticsNo Action Indicated (NAI)3009637528
Sep 29, 2015Newark, DEDrugsNo Action Indicated (NAI)1000307071
Jul 7, 2015Harrisburg, PAFood/CosmeticsNo Action Indicated (NAI)3004695776
May 16, 2014Louisville, KYDevicesNo Action Indicated (NAI)3006759904
Oct 11, 2011Memphis, TNDrugsNo Action Indicated (NAI)3004521773
Jan 18, 2011Decatur, GADrugsNo Action Indicated (NAI)3004563693
Nov 3, 2010Webster, NYFood/CosmeticsNo Action Indicated (NAI)3000205218
Oct 27, 2010Harrisburg, PADrugsNo Action Indicated (NAI)3004695776
Dec 16, 2009San Juan, PRDrugsNo Action Indicated (NAI)3004564305
Aug 26, 2009Memphis, TNDrugsNo Action Indicated (NAI)3004521773

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 3019946577Fairdale, KY1Oct 30, 2025
FEI 3006759904Louisville, KY6Jul 24, 2023
FEI 3014367401Durham, NC1Jun 29, 2023
FEI 3004927096Malden, MA1Jan 22, 2020
FEI 3004695776Harrisburg, PA4Sep 21, 2018
FEI 3009637528Eastvale, CA1Jun 15, 2016
FEI 1000307071Newark, DE1Sep 29, 2015
FEI 3004521773Memphis, TN2Oct 11, 2011
FEI 3004563693Decatur, GA2Jan 18, 2011
FEI 3000205218Webster, NY2Nov 3, 2010
FEI 3004564305San Juan, PR1Dec 16, 2009

FDA data resources

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