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GREEN BOY GROUP

FDA Regulatory Profile

GREEN BOY GROUP has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 29, 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
Jul 29, 2026Los Angeles, CAFood/CosmeticsVoluntary Action Indicated (VAI)3012980467
Mar 13, 2024Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3012980467
Feb 15, 2023Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3012980467
Jul 21, 2021Los Angeles, CAFood/CosmeticsVoluntary Action Indicated (VAI)3012980467

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 3012980467Los Angeles, CA4Jul 29, 2026

FDA data resources

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