Anjan Drug Private Limited

FDA Regulatory Profile

Anjan Drug Private Limited has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 11, 2025 · 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
Inspections7Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 11, 2025Alathur, IndiaDrugsNo Action Indicated (NAI)3005782924
Jan 31, 2020Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3005782924
Aug 16, 2019Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3005782924
Jul 19, 2018Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3005782924
Sep 16, 2016Gummidipoodi, IndiaDrugsVoluntary Action Indicated (VAI)3009402416
Jan 22, 2016Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3005782924
Apr 11, 2013Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3005782924

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 3005782924Alathur, India6Jul 11, 2025
FEI 3009402416Gummidipoodi, India1Sep 16, 2016

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