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The Vapor Craft LLC

FDA Regulatory Profile

The Vapor Craft LLC has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Jan 5, 2023 · NAI

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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
Inspections3Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 5, 2023Columbus, GATobaccoNo Action Indicated (NAI)3010335580
Mar 30, 2022Columbus, GATobaccoOfficial Action Indicated (OAI)3010335580
Jul 19, 2021Columbus, GATobaccoOfficial Action Indicated (OAI)3010335580

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 3010335580Columbus, GA3Jan 5, 2023

FDA data resources

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