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Eqm Research, Inc.

FDA Regulatory Profile

Eqm Research, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

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

Latest inspection: Jan 24, 2019 · NAI
Latest 510(k): Nov 26, 1996

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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	1	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	2	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

Eqm Research, 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	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	1	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

2 inspections from Feb 15, 2017 to Jan 24, 2019.

Date	Site	Product	Classification	FEI
Jan 24, 2019	Cheviot, OH	Devices	No Action Indicated (NAI)	3003502294
Feb 15, 2017	Cheviot, OH	Devices	Voluntary Action Indicated (VAI)	3003502294

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 3003502294	Cheviot, OH	2	Jan 24, 2019

Recent 510(k) clearances

1 510(k) clearance on Nov 26, 1996.

K-Number	Device	Date
K961656	TEST-MATE CHE CHOLINESTERASE TEST SYSTEM	Nov 26, 1996

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