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Augello Enterprises, LLC

FDA Regulatory Profile

Augello Enterprises, LLC 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 "Augello Enterprises, LLC" and its spelling variant "Augello Enterprises".

Latest inspection: Feb 16, 2024 · 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	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

Augello Enterprises, LLC'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	1	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	2	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

7 inspections from Apr 16, 2012 to Feb 16, 2024.

Date	Site	Product	Classification	FEI
Feb 16, 2024	Long Beach, CA	Food/Cosmetics	No Action Indicated (NAI)	3009276442
May 12, 2021	San Pedro, CA	Food/Cosmetics	No Action Indicated (NAI)	3013902160
May 7, 2021	Long Beach, CA	Food/Cosmetics	No Action Indicated (NAI)	3009276442
Feb 21, 2018	San Pedro, CA	Food/Cosmetics	No Action Indicated (NAI)	3013902160
Nov 4, 2016	San Pedro, CA	Food/Cosmetics	No Action Indicated (NAI)	3013902160
Jan 23, 2015	Long Beach, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3009276442
Apr 16, 2012	Long Beach, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3009276442

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

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3009276442	Long Beach, CA	4	Feb 16, 2024
FEI 3013902160	San Pedro, CA	3	May 12, 2021

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