Tissue Transplant Technology, Ltd.

FDA Regulatory Profile

Tissue Transplant Technology, Ltd. has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
May 3, 2024 · VAI

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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
Inspections9Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 3, 2024San Antonio, TXBiologicsVoluntary Action Indicated (VAI)3000779542
Feb 18, 2022San Antonio, TXBiologicsVoluntary Action Indicated (VAI)3000779542
Apr 19, 2018San Antonio, TXBiologicsOfficial Action Indicated (OAI)3000779542
Aug 9, 2017San Antonio, TXBiologicsNo Action Indicated (NAI)3000779542
Jun 8, 2015San Antonio, TXBiologicsNo Action Indicated (NAI)3000779542
Feb 25, 2014San Antonio, TXBiologicsNo Action Indicated (NAI)3000779542
Oct 19, 2012San Antonio, TXBiologicsNo Action Indicated (NAI)3000779542
May 25, 2012San Antonio, TXBiologicsVoluntary Action Indicated (VAI)3000779542
Feb 17, 2011San Antonio, TXBiologicsNo Action Indicated (NAI)3000779542

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 3000779542San Antonio, TX9May 3, 2024

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