Florida Institute For Reproductive Sciences And Technologies

FDA Regulatory Profile

Florida Institute For Reproductive Sciences And Technologies has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 19, 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 actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 19, 2025Weston, FLBiologicsNo Action Indicated (NAI)3004516706
Oct 6, 2022Weston, FLBiologicsNo Action Indicated (NAI)3004516706
Aug 11, 2017Weston, FLBiologicsNo Action Indicated (NAI)3004516706
Feb 10, 2017Weston, FLBiologicsOfficial Action Indicated (OAI)3004516706
Jan 22, 2016Weston, FLBiologicsOfficial Action Indicated (OAI)3004516706
Sep 9, 2014Weston, FLBiologicsVoluntary Action Indicated (VAI)3004516706

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 3004516706Weston, FL6Aug 19, 2025

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