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Tecomet, Inc.

FDA Regulatory Profile

Tecomet, Inc. has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record.

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

Latest inspection: Feb 19, 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	18	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

Tecomet, 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	1	0	0	0	0
2025	0	0	0	0	0
2024	2	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	3	0	0	0	0
2019	2	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

18 inspections from Dec 23, 2008 to Feb 19, 2026.

Date	Site	Product	Classification	FEI
Feb 19, 2026	Kenosha, WI	Devices	No Action Indicated (NAI)	1000306694
Nov 12, 2024	Woburn, MA	Devices	No Action Indicated (NAI)	3003018882
Apr 18, 2024	Boulder, CO	Devices	Voluntary Action Indicated (VAI)	3007137928
Jul 26, 2023	Kenosha, WI	Devices	No Action Indicated (NAI)	1000306694
Jan 17, 2020	Woburn, MA	Devices	No Action Indicated (NAI)	3003018882
Jan 13, 2020	Wilmington, MA	Devices	Voluntary Action Indicated (VAI)	3005226664
Jan 9, 2020	Wilmington, MA	Devices	Voluntary Action Indicated (VAI)	3001451451
Nov 15, 2019	Boulder, CO	Devices	No Action Indicated (NAI)	3007137928
May 7, 2019	Hillburn, NY	Devices	Voluntary Action Indicated (VAI)	3013501169
Jan 12, 2017	Kenosha, WI	Devices	No Action Indicated (NAI)	1000306694
Oct 9, 2015	Boulder, CO	Devices	Voluntary Action Indicated (VAI)	3007137928
Sep 23, 2015	Wilmington, MA	Devices	Voluntary Action Indicated (VAI)	3001451451
Aug 19, 2015	Woburn, MA	Devices	Voluntary Action Indicated (VAI)	3003018882
Jan 20, 2012	Kenosha, WI	Devices	No Action Indicated (NAI)	1000306694
Oct 13, 2010	Kenosha, WI	Devices	No Action Indicated (NAI)	1000306694
May 13, 2010	Wilmington, MA	Devices	No Action Indicated (NAI)	3001451451
May 13, 2010	Woburn, MA	Devices	No Action Indicated (NAI)	3003018882
Dec 23, 2008	Woburn, MA	Devices	Voluntary Action Indicated (VAI)	3003018882

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means 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

6 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 1000306694	Kenosha, WI	5	Feb 19, 2026
FEI 3003018882	Woburn, MA	5	Nov 12, 2024
FEI 3007137928	Boulder, CO	3	Apr 18, 2024
FEI 3005226664	Wilmington, MA	1	Jan 13, 2020
FEI 3001451451	Wilmington, MA	3	Jan 9, 2020
FEI 3013501169	Hillburn, NY	1	May 7, 2019

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