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IVF Michigan, P.C.

FDA Regulatory Profile

IVF Michigan, P.C. has 0 FDA recalls, 20 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
Inspections20Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2025Saginaw, MIBiologicsNo Action Indicated (NAI)3006524198
Jul 17, 2025Ypsilanti, MIBiologicsNo Action Indicated (NAI)3006524208
Jul 17, 2025Dearborn, MIBiologicsNo Action Indicated (NAI)3006524185
Sep 26, 2024Sylvania, OHBiologicsNo Action Indicated (NAI)3011816272
May 14, 2024Grand Blanc, MIBiologicsNo Action Indicated (NAI)3025960441
Dec 4, 2019Dearborn, MIBiologicsNo Action Indicated (NAI)3006524185
Dec 4, 2019Saginaw, MIBiologicsNo Action Indicated (NAI)3006524198
Dec 4, 2019Ypsilanti, MIBiologicsNo Action Indicated (NAI)3006524208
Aug 13, 2019East Lansing, MIBiologicsNo Action Indicated (NAI)3014620680
Mar 29, 2019Sylvania, OHBiologicsNo Action Indicated (NAI)3011816272
Mar 24, 2017Dearborn, MIBiologicsNo Action Indicated (NAI)3006524185
Mar 24, 2017Saginaw, MIBiologicsNo Action Indicated (NAI)3006524198
Mar 24, 2017Ypsilanti, MIBiologicsNo Action Indicated (NAI)3006524208
Dec 14, 2016Sylvania, OHBiologicsNo Action Indicated (NAI)3011816272
Dec 22, 2014Ypsilanti, MIBiologicsNo Action Indicated (NAI)3006524208
Dec 22, 2014Saginaw, MIBiologicsNo Action Indicated (NAI)3006524198
Dec 22, 2014Dearborn, MIBiologicsNo Action Indicated (NAI)3006524185
Jul 31, 2012Saginaw, MIBiologicsNo Action Indicated (NAI)3006524198
Jul 31, 2012Dearborn, MIBiologicsNo Action Indicated (NAI)3006524185
Jul 31, 2012Ypsilanti, MIBiologicsNo Action Indicated (NAI)3006524208

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 3006524185Dearborn, MI5Jul 17, 2025
FEI 3006524198Saginaw, MI5Jul 17, 2025
FEI 3006524208Ypsilanti, MI5Jul 17, 2025
FEI 3011816272Sylvania, OH3Sep 26, 2024
FEI 3025960441Grand Blanc, MI1May 14, 2024
FEI 3014620680East Lansing, MI1Aug 13, 2019

FDA data resources

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