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ALS Group USA, Corp

FDA Regulatory Profile

ALS Group USA, Corp has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "ALS Group USA, Corp" and its spelling variant "Als Group Usa".

Latest inspection: Sep 4, 2026 · 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	9	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

ALS Group USA, Corp'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	1	0	0	0	0
2025	0	0	0	0	0
2024	0	0	0	0	0
2023	1	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	2	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

9 inspections from Jan 28, 2010 to Sep 4, 2026.

Date	Site	Product	Classification	FEI
Sep 4, 2026	Torrance, CA	Drugs	Voluntary Action Indicated (VAI)	2027219
Jun 5, 2023	Torrance, CA	Drugs	Voluntary Action Indicated (VAI)	2027219
Mar 23, 2022	Houston, TX	Drugs	No Action Indicated (NAI)	3012816064
Aug 20, 2018	Phoenix, AZ	Drugs	No Action Indicated (NAI)	3005630502
Feb 16, 2018	Torrance, CA	Drugs	Voluntary Action Indicated (VAI)	2027219
Feb 6, 2017	Houston, TX	Drugs	Voluntary Action Indicated (VAI)	3012816064
Jun 18, 2014	Torrance, CA	Drugs	No Action Indicated (NAI)	2027219
Mar 1, 2012	Torrance, CA	Drugs	No Action Indicated (NAI)	2027219
Jan 28, 2010	Torrance, CA	Drugs	Voluntary Action Indicated (VAI)	2027219

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

3 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 2027219	Torrance, CA	6	Sep 4, 2026
FEI 3012816064	Houston, TX	2	Mar 23, 2022
FEI 3005630502	Phoenix, AZ	1	Aug 20, 2018

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