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Grindhouse Eliquid LLC

FDA Regulatory Profile

Grindhouse Eliquid 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 "Grindhouse Eliquid LLC" and its spelling variant "Grindhouse Eliquid".

Latest inspection: Jun 27, 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 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	2	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Grindhouse Eliquid 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	1
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

1 inspection on Jun 27, 2019.

Date	Site	Product	Classification	FEI
Jun 27, 2019	Poplar Bluff, MO	Tobacco	No Action Indicated (NAI)	3012955428

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 Grindhouse Eliquid 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, Jul 29, 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 3012955428	Poplar Bluff, MO	1	Jun 27, 2019

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