Azenta Life Sciences, Inc

FDA Regulatory Profile

Azenta Life Sciences, Inc has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 12, 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
Inspections7Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 12, 2025Indianapolis, INBiologicsNo Action Indicated (NAI)3004757032
Aug 22, 2019Indianapolis, INDrugsNo Action Indicated (NAI)3004757032
Jul 6, 2018Indianapolis, INBiologicsVoluntary Action Indicated (VAI)3004757032
Aug 5, 2016Indianapolis, INBiologicsNo Action Indicated (NAI)3004757032
Jun 5, 2014Indianapolis, INBiologicsNo Action Indicated (NAI)3004757032
Jul 25, 2012Indianapolis, INBiologicsNo Action Indicated (NAI)3004757032
Jan 14, 2009Indianapolis, INBiologicsNo Action Indicated (NAI)3004757032

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 3004757032Indianapolis, IN7Aug 12, 2025

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