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STL Fertility

FDA Regulatory Profile

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

Latest inspection
Aug 21, 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 21, 2025Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689
Oct 29, 2019Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689
Mar 7, 2017Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689
Apr 15, 2015Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689
Apr 3, 2013Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689
Aug 25, 2009Creve Coeur, MOBiologicsNo Action Indicated (NAI)3003934689

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 3003934689Creve Coeur, MO6Aug 21, 2025

FDA data resources

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