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Cosmic Fog Vapors Operating Company, LLC

FDA Regulatory Profile

Cosmic Fog Vapors Operating Company, LLC has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 2 compliance actions on record.

What these totals cover: FDA records filed under the name "Cosmic Fog Vapors Operating Company, LLC" and its spelling variant "Cosmic Fog Vapors Operating Company".

Latest inspection: Feb 12, 2019 · NAI

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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	1	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	2	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Cosmic Fog Vapors Operating Company, LLC'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	0	0
2025	0	0
2024	0	0
2023	0	0
2022	0	0
2021	0	1
2020	0	0
2019	1	0
2018	0	1
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

1 inspection on Feb 12, 2019.

Date	Site	Product	Classification	FEI
Feb 12, 2019	Santa Ana, CA	Tobacco	No Action Indicated (NAI)	3011857658

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 Cosmic Fog Vapors Operating Company, LLC: 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, Dec 20, 2021.

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

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3011857658	Santa Ana, CA	1	Feb 12, 2019

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