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Megafine Pharma (P) Limited

FDA Regulatory Profile

Megafine Pharma (P) Limited has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
May 12, 2023 · 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
Inspections10Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 12, 2023Vapi, IndiaDrugsVoluntary Action Indicated (VAI)3006688078
Jan 24, 2023Nashik, IndiaDrugsVoluntary Action Indicated (VAI)3005694111
Mar 6, 2020Nashik, IndiaDrugsOfficial Action Indicated (OAI)3005694111
Feb 21, 2020Vapi, IndiaDrugsOfficial Action Indicated (OAI)3006688078
Jun 15, 2018Vapi, IndiaDrugsOfficial Action Indicated (OAI)3006688078
May 12, 2018Nashik, IndiaDrugsOfficial Action Indicated (OAI)3005694111
Sep 23, 2016Vapi, IndiaDrugsOfficial Action Indicated (OAI)3006688078
May 15, 2015Nashik, IndiaVeterinaryOfficial Action Indicated (OAI)3005694111
Mar 13, 2013Vapi, IndiaDrugsVoluntary Action Indicated (VAI)3006688078
Jun 2, 2011Nashik, IndiaDrugsNo Action Indicated (NAI)3005694111

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 3006688078Vapi, India5May 12, 2023
FEI 3005694111Nashik, India5Jan 24, 2023

FDA data resources

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