Montgomery Fertility Center

FDA Regulatory Profile

Montgomery Fertility Center has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jan 17, 2024 · 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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 17, 2024Rockville, MDBiologicsNo Action Indicated (NAI)3009658676
Jul 28, 2022Rockville, MDBiologicsNo Action Indicated (NAI)3009658676
Aug 11, 2021Rockville, MDBiologicsNo Action Indicated (NAI)3009658676
Jan 21, 2020Rockville, MDBiologicsOfficial Action Indicated (OAI)3009658676
Dec 20, 2017Rockville, MDBiologicsNo Action Indicated (NAI)3009658676
Aug 1, 2016Rockville, MDBiologicsNo Action Indicated (NAI)3009658676
Dec 4, 2013Silver Spring, MDBiologicsNo Action Indicated (NAI)3009984103
Oct 25, 2012Rockville, MDBiologicsNo Action Indicated (NAI)3009658676

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 3009658676Rockville, MD7Jan 17, 2024
FEI 3009984103Silver Spring, MD1Dec 4, 2013

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