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AVFlight Of Traverse City Co. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Latest inspection NAI · Aug 30, 2021
No warning letters matched by name

Inspections 2

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

AVFlight Of Traverse City Co. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "AVFlight Of Traverse City Co." is on file.

What these totals cover: FDA records filed under the name "AVFlight Of Traverse City Co." and its spelling variant "Avflight Of Traverse City".

Latest inspection: Aug 30, 2021 · NAI

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	2	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

AVFlight Of Traverse City Co.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

AVFlight Of Traverse City Co.: FDA inspections per year

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	0	0	0	0	0
2022	0	0	0	0	0
2021	1	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.

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Recent FDA inspections

2 inspections from Sep 20, 2017 to Aug 30, 2021.

Date	Site	Product	Classification	FEI
Aug 30, 2021	Traverse City, MI	Food/Cosmetics	No Action Indicated (NAI)	3013859838
Sep 20, 2017	Traverse City, MI	Food/Cosmetics	No Action Indicated (NAI)	3013859838

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 3013859838	Traverse City, MI	2	Aug 30, 2021

AVFlight Of Traverse City Co. and the FDA: common questions

Has AVFlight Of Traverse City Co. received an FDA warning letter?

No FDA warning letter addressed to the name "AVFlight Of Traverse City Co." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has AVFlight Of Traverse City Co. received an FDA Form 483?

FDA has not published a Form 483 for "AVFlight Of Traverse City Co." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect AVFlight Of Traverse City Co.?

The most recent FDA inspection on file ended Aug 30, 2021 at Traverse City, MI and was classified NAI. FDA has 2 inspections of AVFlight Of Traverse City Co. on file.

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