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Anicare Pharmaceuticals Pvt Ltd.

FDA Regulatory Profile

Anicare Pharmaceuticals Pvt Ltd. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jan 20, 2023 · OAI

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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
Inspections3Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 20, 2023Navi Mumbai, IndiaDrugsOfficial Action Indicated (OAI)3007450508
Aug 3, 2018Navi Mumbai, IndiaDrugsOfficial Action Indicated (OAI)3007450508
Jul 14, 2016Navi Mumbai, IndiaDrugsVoluntary Action Indicated (VAI)3007450508

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 3007450508Navi Mumbai, India3Jan 20, 2023

FDA data resources

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