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Jubilant Pharmova Limited

FDA Regulatory Profile

Jubilant Pharmova Limited has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 13, 2022 · 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
Inspections5Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 13, 2022Mysore, IndiaDrugsVoluntary Action Indicated (VAI)3003144728
Dec 18, 2018Mysore, IndiaDrugsOfficial Action Indicated (OAI)3003144728
Oct 27, 2017Mysore, IndiaDrugsVoluntary Action Indicated (VAI)3003144728
Oct 16, 2015Mysore, IndiaDrugsNo Action Indicated (NAI)3003144728
May 31, 2012Mysore, IndiaDrugsVoluntary Action Indicated (VAI)3003144728

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 3003144728Mysore, India5Dec 13, 2022

FDA data resources

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