IVF Michigan

FDA Regulatory Profile

IVF Michigan has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 17, 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
Jul 17, 2025Bloomfield Hills, MIBiologicsNo Action Indicated (NAI)3010929692
Jul 17, 2025Macomb, MIBiologicsNo Action Indicated (NAI)3013526565
Dec 4, 2019Bloomfield Hills, MIBiologicsNo Action Indicated (NAI)3010929692
Dec 4, 2019Macomb, MIBiologicsNo Action Indicated (NAI)3013526565
Mar 6, 2018Macomb, MIBiologicsNo Action Indicated (NAI)3013526565
Mar 24, 2017Bloomfield Hills, MIBiologicsNo Action Indicated (NAI)3010929692
Dec 22, 2014Bloomfield Hills, MIBiologicsNo Action Indicated (NAI)3010929692

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 3010929692Bloomfield Hills, MI4Jul 17, 2025
FEI 3013526565Macomb, MI3Jul 17, 2025

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