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Moehs Cantabra, S.L.

FDA Regulatory Profile

Moehs Cantabra, S.L. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 1 compliance action on record.

What these totals cover: FDA records filed under the name "Moehs Cantabra, S.L." and its spelling variant "Moehs Cantabra, S.L".

Latest inspection: Jul 17, 2025 · 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	6	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Moehs Cantabra, S.L.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	1	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	1	0	0	0	0
2017	0	0	0	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

6 inspections from Dec 17, 2010 to Jul 17, 2025.

Date	Site	Product	Classification	FEI
Jul 17, 2025	Polanco, Spain	Drugs	Voluntary Action Indicated (VAI)	3004096632
Nov 24, 2022	Polanco, Spain	Drugs	Voluntary Action Indicated (VAI)	3004096632
Jan 18, 2018	Polanco, Spain	Drugs	Voluntary Action Indicated (VAI)	3004096632
Oct 9, 2015	Polanco, Spain	Drugs	Voluntary Action Indicated (VAI)	3004096632
Mar 30, 2012	Polanco, Spain	Drugs	Voluntary Action Indicated (VAI)	3004096632
Dec 17, 2010	Polanco, Spain	Drugs	Official Action Indicated (OAI)	3004096632

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 1 compliance action under Moehs Cantabra, S.L.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Apr 14, 2011.

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 3004096632	Polanco, Spain	6	Jul 17, 2025

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