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Lupin Research Inc

FDA Regulatory Profile

Lupin Research Inc has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 26, 2020 · VAI

Newer recall under related name Lupin Pharmaceuticals: Aug 3, 2026, D-0789-2026.

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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
Inspections1Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Lupin Pharmaceuticals
Same company group		123040Aug 3, 2026 (D-0789-2026)
Lupin Limited
Same company group		40425Nov 17, 2017 (D-0092-2018)
Lupin
Same company group		0050—

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 26, 2020Coral Springs, FLDrugsVoluntary Action Indicated (VAI)3014650220

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 3014650220Coral Springs, FL1Feb 26, 2020

FDA data resources

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