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Allegiant Air IND

FDA Regulatory Profile

Allegiant Air IND has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Allegiant Air IND".

Latest inspection: May 18, 2026 · 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	8	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

Allegiant Air IND'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	0	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

8 inspections from Jan 19, 2016 to May 18, 2026.

Date	Site	Product	Classification	FEI
May 18, 2026	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Jan 17, 2017	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Dec 9, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Oct 7, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
May 16, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Apr 4, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Apr 4, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086
Jan 19, 2016	Indianapolis, IN	Food/Cosmetics	No Action Indicated (NAI)	3012060086

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 3012060086	Indianapolis, IN	8	May 18, 2026

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