Jubilant Generics Limited

FDA Regulatory Profile

Jubilant Generics Limited has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 2, 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
Inspections8Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 2, 2024Roorkee, IndiaDrugsVoluntary Action Indicated (VAI)3006895982
Aug 1, 2022Roorkee, IndiaDrugsOfficial Action Indicated (OAI)3006895982
Mar 12, 2021Roorkee, IndiaDrugsOfficial Action Indicated (OAI)3006895982
Nov 6, 2019Roorkee, IndiaDrugsOfficial Action Indicated (OAI)3006895982
Mar 23, 2017Roorkee, IndiaDrugsNo Action Indicated (NAI)3006895982
Apr 8, 2016Roorkee, IndiaDrugsVoluntary Action Indicated (VAI)3006895982
Mar 13, 2015Roorkee, IndiaDrugsVoluntary Action Indicated (VAI)3006895982
Mar 1, 2013Roorkee, IndiaDrugsVoluntary Action Indicated (VAI)3006895982

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 3006895982Roorkee, India8Feb 2, 2024

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