Reproductive Specialty Center Ltd

FDA Regulatory Profile

Reproductive Specialty Center Ltd has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 13, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 13, 2025Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984
Dec 10, 2019Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984
Dec 6, 2017Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984
Nov 30, 2015Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984
Nov 1, 2013Milwaukee, WIBiologicsVoluntary Action Indicated (VAI)3003981984
Jan 25, 2012Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984
Jan 26, 2010Milwaukee, WIBiologicsNo Action Indicated (NAI)3003981984

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 3003981984Milwaukee, WI7Jun 13, 2025

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