Alabama Fertility Specialists, PC

FDA Regulatory Profile

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

Latest inspection
Sep 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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 17, 2025Homewood, ALBiologicsNo Action Indicated (NAI)3005056987
Mar 15, 2023Homewood, ALBiologicsVoluntary Action Indicated (VAI)3005056987
Aug 22, 2019Homewood, ALBiologicsNo Action Indicated (NAI)3005056987
May 4, 2017Homewood, ALBiologicsVoluntary Action Indicated (VAI)3005056987
Nov 19, 2014Homewood, ALBiologicsNo Action Indicated (NAI)3005056987
Jan 25, 2010Homewood, ALBiologicsNo Action Indicated (NAI)3005056987

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 3005056987Homewood, AL6Sep 17, 2025

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