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Voyant Beauty, Inc.

FDA Regulatory Profile

Voyant Beauty, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 30, 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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 30, 2025Etobicoke, CanadaDrugsVoluntary Action Indicated (VAI)1000251162
Oct 25, 2019Etobicoke, CanadaDrugsNo Action Indicated (NAI)1000251162
Jun 8, 2017Etobicoke, CanadaDevicesNo Action Indicated (NAI)1000251162
Dec 16, 2016Etobicoke, CanadaDrugsVoluntary Action Indicated (VAI)1000251162
May 30, 2014Etobicoke, CanadaDrugsVoluntary Action Indicated (VAI)1000251162
Mar 13, 2014Etobicoke, CanadaDevicesVoluntary Action Indicated (VAI)1000251162
Apr 27, 2012Etobicoke, CanadaDrugsNo Action Indicated (NAI)1000251162
Aug 13, 2010Etobicoke, CanadaDrugsNo Action Indicated (NAI)1000251162

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 1000251162Etobicoke, Canada8May 30, 2025

FDA data resources

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