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Induction Therapies, LLC FDA Record

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

Latest inspection NAI · Aug 8, 2025
Last warning letter 2021

Inspections 4

1 OAI

Recalls 0 0 Class I

Warning letters 1 Latest Nov 23, 2021

510(k) clearances 1 Latest Oct 21, 2022

Induction Therapies, LLC has 0 FDA recalls, 4 inspections, 1 510(k) clearance and 1 compliance action on record. FDA has issued 1 warning letter to Induction Therapies, LLC, the most recent on Nov 23, 2021.

What these totals cover: FDA records filed under the name "Induction Therapies, LLC" and its spelling variant "Induction Therapies".

Latest inspection: Aug 8, 2025 · NAI
Latest 510(k): Oct 21, 2022

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	1	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	4	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Induction Therapies, LLC's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Induction Therapies, LLC: FDA inspections per year

Year	Inspections	OAI	Warning letters
2026	0	0	0
2025	1	0	0
2024	1	0	0
2023	0	0	0
2022	0	0	0
2021	1	1	1
2020	0	0	0
2019	1	0	0
2018	0	0	0
2017	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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Induction Therapies, LLC FDA Warning Letters

1 warning letter on Nov 23, 2021.

Issued	Subject	Issuing office	Close-out letter
Nov 23, 2021 · Letter on fda.gov	Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device	Center for Devices and Radiological Health	Nov 8, 2022

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

4 inspections from Mar 21, 2019 to Aug 8, 2025.

Date	Site	Product	Classification	FEI
Aug 8, 2025	Louisville, KY	Devices	No Action Indicated (NAI)	3014171792
Oct 18, 2024	Louisville, KY	Drugs	Voluntary Action Indicated (VAI)	3014171792
Jun 29, 2021	Louisville, KY	Devices	Official Action Indicated (OAI)	3014171792
Mar 21, 2019	Louisville, KY	Devices	Voluntary Action Indicated (VAI)	3014171792

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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Induction Therapies, LLC: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Nov 23, 2021.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3014171792	Louisville, KY	4	Aug 8, 2025

Recent 510(k) clearances

1 510(k) clearance on Oct 21, 2022.

K-Number	Device	Date
K222199	Collagen P.I.N. (Percutaneous Induction Needling)	Oct 21, 2022

Induction Therapies, LLC and the FDA: common questions

Has Induction Therapies, LLC received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Induction Therapies, LLC. The most recent is dated Nov 23, 2021, with the subject "Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device".

Has Induction Therapies, LLC received an FDA Form 483?

FDA has not published a Form 483 for "Induction Therapies, LLC" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Induction Therapies, LLC?

The most recent FDA inspection on file ended Aug 8, 2025 at Louisville, KY and was classified NAI. FDA has 4 inspections of Induction Therapies, LLC on file, 1 of them classified OAI (official action indicated).

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