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A.I.G Technologies Inc.

FDA Regulatory Profile

A.I.G Technologies Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
May 16, 2025 · VAI

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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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 16, 2025Deerfield Beach, FLDrugsVoluntary Action Indicated (VAI)3003511617
Sep 25, 2019Deerfield Beach, FLDrugsVoluntary Action Indicated (VAI)3003511617
Nov 17, 2015Deerfield Beach, FLDrugsOfficial Action Indicated (OAI)3003511617
Nov 20, 2012Deerfield Beach, FLFood/CosmeticsNo Action Indicated (NAI)3003511617
Jul 1, 2011Deerfield Beach, FLDrugsVoluntary Action Indicated (VAI)3003511617

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 3003511617Deerfield Beach, FL5May 16, 2025

FDA data resources

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