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Rip It Vapors

FDA Regulatory Profile

Rip It Vapors has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Feb 15, 2024 · 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
Feb 15, 2024Kennett Square, PATobaccoNo Action Indicated (NAI)3013924502
Jul 13, 2022Kennett Square, PATobaccoOfficial Action Indicated (OAI)3013924502
Aug 12, 2021Kennett Square, PATobaccoOfficial Action Indicated (OAI)3013924502

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 3013924502Kennett Square, PA3Feb 15, 2024

FDA data resources

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