Aimani International LTD

FDA Regulatory Profile

Aimani International LTD has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 19, 2026 · VAI

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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
Inspections4Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 19, 2026Long Island City, NYFood/CosmeticsVoluntary Action Indicated (VAI)3001650701
Oct 22, 2020Long Island City, NYFood/CosmeticsVoluntary Action Indicated (VAI)3001650701
Jun 1, 2017Long Island City, NYFood/CosmeticsVoluntary Action Indicated (VAI)3001650701
May 10, 2016Long Island City, NYFood/CosmeticsVoluntary Action Indicated (VAI)3001650701

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 3001650701Long Island City, NY4Oct 19, 2026

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