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QED, Inc. FDA Record

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

QED, Inc. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "QED, Inc." is on file.

What these totals cover: FDA records filed under the name "QED, Inc." and its spelling variant "Qed".

Latest inspection: Apr 11, 2025 · VAI

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	3	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

QED, Inc.'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	1	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	1	0	0	0	0
2019	0	0	0	0	0
2018	0	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.

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Recent FDA inspections

3 inspections from Jan 21, 2011 to Apr 11, 2025.

Date	Site	Product	Classification	FEI
Apr 11, 2025	Lexington, KY	Devices	Voluntary Action Indicated (VAI)	1037039
Feb 26, 2020	Lexington, KY	Devices	Voluntary Action Indicated (VAI)	1037039
Jan 21, 2011	Lexington, KY	Devices	Voluntary Action Indicated (VAI)	1037039

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 1037039	Lexington, KY	3	Apr 11, 2025

QED, Inc. and the FDA: common questions

Has QED, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "QED, Inc." 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 QED, Inc. received an FDA Form 483?

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

When did the FDA last inspect QED, Inc.?

The most recent FDA inspection on file ended Apr 11, 2025 at Lexington, KY and was classified VAI. FDA has 3 inspections of QED, Inc. on file.

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