Home / Companies / Dishman Carbogen Amcis Limited

Dishman Carbogen Amcis Limited

FDA Regulatory Profile

Dishman Carbogen Amcis Limited has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 12, 2025 · NAI

Reviewing Dishman Carbogen Amcis 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 Dishman Carbogen Amcis 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 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 12, 2025Ahmedabad, IndiaDrugsNo Action Indicated (NAI)1000607691
Mar 7, 2024Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3004161218
Feb 15, 2019Ahmedabad, IndiaDrugsNo Action Indicated (NAI)1000607691
Oct 26, 2018Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3004161218
Jul 8, 2016Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3004161218
Oct 22, 2015Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)1000607691
May 2, 2013Ahmedabad, IndiaDrugsNo Action Indicated (NAI)1000607691
Mar 17, 2012Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3004161218
Feb 4, 2010Ahmedabad, IndiaDrugsNo Action Indicated (NAI)1000607691

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 1000607691Ahmedabad, India5Jun 12, 2025
FEI 3004161218Ahmedabad, India4Mar 7, 2024

FDA data resources

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