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Hello Life, Inc

FDA Regulatory Profile

Hello Life, Inc has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 2, 2021 · 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
Inspections6Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 2, 2021Grand Rapids, MIDrugsVoluntary Action Indicated (VAI)3009727070
Mar 7, 2019Grand Rapids, MIFood/CosmeticsOfficial Action Indicated (OAI)3009727070
Mar 10, 2017Grand Rapids, MIFood/CosmeticsNo Action Indicated (NAI)3009727070
Jun 4, 2014Grand Rapids, MIDrugsVoluntary Action Indicated (VAI)3009727070
Jun 4, 2014Grand Rapids, MIVeterinaryVoluntary Action Indicated (VAI)3009727070
Oct 21, 2011Grand Rapids, MIFood/CosmeticsVoluntary Action Indicated (VAI)3009727070

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 3009727070Grand Rapids, MI6Sep 2, 2021

FDA data resources

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