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Nelson Laboratories, LLC

FDA Regulatory Profile

Nelson Laboratories, LLC has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 26, 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
Sep 26, 2025Itasca, ILDrugsVoluntary Action Indicated (VAI)3000717698
Jul 30, 2025Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3000233845
Jun 2, 2023Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)3000233845
Nov 9, 2021Salt Lake City, UTBiologicsNo Action Indicated (NAI)3000233845
Nov 8, 2018Itasca, ILDrugsNo Action Indicated (NAI)3000717698
Mar 30, 2018Salt Lake City, UTDrugsNo Action Indicated (NAI)3000233845
Feb 23, 2018Salt Lake City, UTBiologicsNo Action Indicated (NAI)3000233845
Apr 15, 2016Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3000233845
Mar 11, 2016Itasca, ILVeterinaryVoluntary Action Indicated (VAI)3000717698
Feb 26, 2016Salt Lake City, UTVeterinaryNo Action Indicated (NAI)3000233845
Jun 25, 2015Salt Lake City, UTDevicesNo Action Indicated (NAI)3000233845
Jan 10, 2014Salt Lake City, UTVeterinaryNo Action Indicated (NAI)3000233845
Jun 12, 2013Itasca, ILFood/CosmeticsNo Action Indicated (NAI)3000717698
Mar 9, 2012Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3000233845
Dec 7, 2011Itasca, ILBiologicsNo Action Indicated (NAI)3000717698
Mar 8, 2011Salt Lake City, UTBiologicsNo Action Indicated (NAI)3000233845
Oct 8, 2010Itasca, ILDrugsNo Action Indicated (NAI)3000717698
Jan 8, 2010Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)3000233845

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 3000717698Itasca, IL6Sep 26, 2025
FEI 3000233845Salt Lake City, UT12Jul 30, 2025

FDA data resources

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