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Allpack Group AG

FDA Regulatory Profile

Allpack Group AG has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Allpack Group AG" and its spelling variant "Allpack Group".

Latest inspection: Apr 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	7	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Allpack Group AG'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	0	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	1	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

7 inspections from Nov 6, 2009 to Apr 28, 2023.

Date	Site	Product	Classification	FEI
Apr 28, 2023	Reinach BL, Switzerland	Drugs	Voluntary Action Indicated (VAI)	3004362706
Jul 7, 2017	Reinach BL, Switzerland	Drugs	No Action Indicated (NAI)	3004362706
Feb 13, 2015	Reinach BL, Switzerland	Drugs	No Action Indicated (NAI)	3004362706
Feb 22, 2013	Reinach BL, Switzerland	Devices	No Action Indicated (NAI)	3004362706
Dec 12, 2012	Reinach BL, Switzerland	Drugs	No Action Indicated (NAI)	3004362706
Nov 21, 2011	Reinach BL, Switzerland	Drugs	No Action Indicated (NAI)	3004362706
Nov 6, 2009	Reinach BL, Switzerland	Devices	Voluntary Action Indicated (VAI)	3004362706

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.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3004362706	Reinach BL, Switzerland	7	Apr 28, 2023

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