Home / Companies / Kumar Organic Products Limited

Kumar Organic Products Limited

FDA Regulatory Profile

Kumar Organic Products Limited has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 22, 2025 · VAI

Reviewing Kumar Organic Products Limited as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Kumar Organic Products Limited yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

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 actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 22, 2025Hassan, IndiaDrugsVoluntary Action Indicated (VAI)3008957541
Jun 13, 2025Anekal Taluk, Bengaluru, IndiaDrugsVoluntary Action Indicated (VAI)3003768909
Apr 21, 2023Vadodara, IndiaDrugsVoluntary Action Indicated (VAI)3009167769
Nov 14, 2019Vadodara, IndiaDrugsOfficial Action Indicated (OAI)3009167769
Feb 8, 2019Anekal Taluk, Bengaluru, IndiaDrugsVoluntary Action Indicated (VAI)3003768909
Jul 20, 2018Hassan, IndiaDrugsNo Action Indicated (NAI)3008957541
Sep 22, 2016Vadodara, IndiaDrugsVoluntary Action Indicated (VAI)3009167769
May 13, 2016Anekal Taluk, Bengaluru, IndiaDrugsVoluntary Action Indicated (VAI)3003768909
Jul 18, 2014Anekal Taluk, Bengaluru, IndiaDrugsVoluntary Action Indicated (VAI)3003768909
Mar 17, 2011Anekal Taluk, Bengaluru, IndiaDrugsVoluntary Action Indicated (VAI)3003768909

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 3008957541Hassan, India2Aug 22, 2025
FEI 3003768909Anekal Taluk, Bengaluru, India5Jun 13, 2025
FEI 3009167769Vadodara, India3Apr 21, 2023

FDA data resources

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