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Lifesource Evanston

FDA Regulatory Profile

Lifesource Evanston has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 13, 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
Inspections6Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 13, 2025Evanston, ILBiologicsNo Action Indicated (NAI)3009382452
Feb 4, 2020Evanston, ILBiologicsNo Action Indicated (NAI)3009382452
May 2, 2018Evanston, ILBiologicsNo Action Indicated (NAI)3009382452
May 31, 2016Evanston, ILBiologicsNo Action Indicated (NAI)3009382452
Feb 20, 2014Evanston, ILBiologicsNo Action Indicated (NAI)3009382452
Apr 17, 2012Evanston, ILBiologicsNo Action Indicated (NAI)3009382452

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 3009382452Evanston, IL6Aug 13, 2025

FDA data resources

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