Vitalabs, Inc.

FDA Regulatory Profile

Vitalabs, Inc. has 1 FDA recall, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
H-0037-2026 · Class II · Jun 13, 2025
Latest inspection
Sep 28, 2023 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
H-0037-2026Class IIvitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black…Jun 13, 2025

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 28, 2023McDonough, GAFood/CosmeticsVoluntary Action Indicated (VAI)1048033
Jun 29, 2022McDonough, GAFood/CosmeticsNo Action Indicated (NAI)1048033
Dec 19, 2018McDonough, GAFood/CosmeticsNo Action Indicated (NAI)1048033
Dec 1, 2016McDonough, GAFood/CosmeticsNo Action Indicated (NAI)1048033
Aug 2, 2016McDonough, GAFood/CosmeticsNo Action Indicated (NAI)1048033
Feb 21, 2014McDonough, GAFood/CosmeticsVoluntary Action Indicated (VAI)1048033

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 1048033McDonough, GA6Sep 28, 2023

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