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Honeywell Safety Products USA, Inc. FDA Record

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

Latest inspection NAI · Sep 16, 2025
No warning letters matched by name

Inspections 4

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Honeywell Safety Products USA, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Honeywell Safety Products USA, Inc." is on file.

What these totals cover: FDA records filed under the name "Honeywell Safety Products USA, Inc." and its spelling variant "Honeywell Safety Products Usa".

Latest inspection: Sep 16, 2025 · 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	4	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

Honeywell Safety Products USA, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Honeywell Safety Products USA, Inc.: FDA inspections per year

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	2	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	1	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

4 inspections from Dec 10, 2018 to Sep 16, 2025.

Date	Site	Product	Classification	FEI
Sep 16, 2025	San Diego, CA	Devices	No Action Indicated (NAI)	3010588332
Nov 9, 2022	San Diego, CA	Devices	No Action Indicated (NAI)	3010588332
Feb 23, 2022	Smithfield, RI	Devices	No Action Indicated (NAI)	3005664148
Dec 10, 2018	San Diego, CA	Devices	No Action Indicated (NAI)	3010588332

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

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3010588332	San Diego, CA	3	Sep 16, 2025
FEI 3005664148	Smithfield, RI	1	Feb 23, 2022

Honeywell Safety Products USA, Inc. and the FDA: common questions

Has Honeywell Safety Products USA, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Honeywell Safety Products USA, 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 Honeywell Safety Products USA, Inc. received an FDA Form 483?

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

When did the FDA last inspect Honeywell Safety Products USA, Inc.?

The most recent FDA inspection on file ended Sep 16, 2025 at San Diego, CA and was classified NAI. FDA has 4 inspections of Honeywell Safety Products USA, Inc. on file.

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