Home / Companies / Alfasigma USA, Inc.

Alfasigma USA, Inc.

FDA Regulatory Profile

Alfasigma USA, Inc. has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
May 21, 2026 · NAI

Reviewing Alfasigma USA, Inc. 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 Alfasigma USA, Inc. 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

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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
Inspections11Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 21, 2026Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
May 16, 2025Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Jul 30, 2024Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Apr 25, 2024Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
May 18, 2023Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Aug 18, 2022Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Aug 14, 2019Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Sep 11, 2018Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
Jun 25, 2018Shreveport, LAFood/CosmeticsNo Action Indicated (NAI)3011104045
May 8, 2014Shreveport, LADrugsNo Action Indicated (NAI)3011104045
Aug 15, 2013Shreveport, LADrugsNo Action Indicated (NAI)3011104045

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 3011104045Shreveport, LA11May 21, 2026

FDA data resources

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