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KingPin Cigarettes, Inc.

FDA Regulatory Profile

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

What these totals cover: FDA records filed under the name "KingPin Cigarettes, Inc." and its spelling variant "Kingpin Cigarettes".

Latest inspection: Jan 16, 2026 · VAI

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	2	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	2	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

KingPin Cigarettes, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	Warning letters
2026	2	1
2025	0	0
2024	0	0
2023	0	1
2022	0	0
2021	0	0
2020	0	0
2019	0	0
2018	0	0
2017	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

2 inspections on Jan 16, 2026.

Date	Site	Product	Classification	FEI
Jan 16, 2026	Atlantic Beach, FL	Tobacco	Voluntary Action Indicated (VAI)	3013842206
Jan 16, 2026	Jacksonville, FL	Tobacco	Voluntary Action Indicated (VAI)	3013841712

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 2 compliance actions under KingPin Cigarettes, Inc.: warning letters, injunctions and seizures. All of them came from FDA's Center for Tobacco Products, which regulates tobacco retailers and manufacturers. They are not drug, medical device or food manufacturing actions.

Most recent: Warning Letter, Mar 30, 2026.

Individual actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3013841712	Jacksonville, FL	1	Jan 16, 2026
FEI 3013842206	Atlantic Beach, FL	1	Jan 16, 2026

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