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Stille AB

FDA Regulatory Profile

Stille AB has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 1 compliance action on record.

What these totals cover: FDA records filed under the name "Stille AB" and its spelling variant "Stille".

Latest inspection: Sep 28, 2023 · 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	3	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

Recent FDA inspections

3 inspections from Aug 12, 2010 to Sep 28, 2023.

Date	Site	Product	Classification	FEI
Sep 28, 2023	Torshalla, Sweden	Devices	Voluntary Action Indicated (VAI)	3003696170
Aug 22, 2013	Torshalla, Sweden	Devices	Voluntary Action Indicated (VAI)	3003696170
Aug 12, 2010	Torshalla, Sweden	Devices	Voluntary Action Indicated (VAI)	3003696170

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 Stille AB: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jan 31, 2014.

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 3003696170	Torshalla, Sweden	3	Sep 28, 2023

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