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LA Vapor Inc

FDA Regulatory Profile

LA Vapor Inc has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
May 29, 2025 · OAI

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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
Inspections2Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 29, 2025Houston, TXTobaccoOfficial Action Indicated (OAI)3030606660
Mar 18, 2024Diamond Bar, CATobaccoOfficial Action Indicated (OAI)3012664238

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 3030606660Houston, TX1May 29, 2025
FEI 3012664238Diamond Bar, CA1Mar 18, 2024

FDA data resources

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