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Houston IVF PA

FDA Regulatory Profile

Houston IVF PA has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 16, 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 16, 2025Houston, TXBiologicsNo Action Indicated (NAI)3004554702
Nov 8, 2022Houston, TXBiologicsNo Action Indicated (NAI)3004554702
Apr 3, 2018Houston, TXBiologicsNo Action Indicated (NAI)3004554702
May 6, 2014Houston, TXBiologicsNo Action Indicated (NAI)3004554702
May 10, 2012Houston, TXBiologicsNo Action Indicated (NAI)3004554702

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 3004554702Houston, TX5Sep 16, 2025

FDA data resources

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