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Lambda Therapeutic Research Ltd.

FDA Regulatory Profile

Lambda Therapeutic Research Ltd. has 0 FDA recalls, 12 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 1, 2026 · 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
Inspections12Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 1, 2026Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764
Jul 18, 2025Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764
Nov 14, 2022Mehsana, IndiaDrugsNo Action Indicated (NAI)3013752226
Nov 2, 2022Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764
Jan 24, 2020Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3005124764
Dec 13, 2019Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764
Aug 2, 2019Navi Mumbai, IndiaDrugsNo Action Indicated (NAI)3006005701
Dec 7, 2018Navi Mumbai, IndiaDrugsNo Action Indicated (NAI)3006005701
Aug 31, 2018Mehsana, IndiaDrugsNo Action Indicated (NAI)3013752226
Apr 27, 2018Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3005124764
Feb 16, 2018Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764
Jun 25, 2014Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005124764

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 3005124764Ahmedabad, India8May 1, 2026
FEI 3013752226Mehsana, India2Nov 14, 2022
FEI 3006005701Navi Mumbai, India2Aug 2, 2019

FDA data resources

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