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Bridor USA Inc. FDA Record

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

Bridor USA Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Bridor USA Inc." is on file.

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

Latest inspection: Jul 23, 2020 · 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	5	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

Bridor USA 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	1	0	0	0	0
2019	0	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.

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Recent FDA inspections

5 inspections from Dec 8, 2009 to Jul 23, 2020.

Date	Site	Product	Classification	FEI
Jul 23, 2020	Bridgeport, CT	Food/Cosmetics	No Action Indicated (NAI)	3004708173
Feb 16, 2017	Vineland, NJ	Food/Cosmetics	No Action Indicated (NAI)	3004894019
Oct 31, 2011	Bridgeport, CT	Food/Cosmetics	No Action Indicated (NAI)	3004708173
Jan 24, 2011	Vineland, NJ	Food/Cosmetics	No Action Indicated (NAI)	3004894019
Dec 8, 2009	Vineland, NJ	Food/Cosmetics	No Action Indicated (NAI)	3004894019

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 3004708173	Bridgeport, CT	2	Jul 23, 2020
FEI 3004894019	Vineland, NJ	3	Feb 16, 2017

Bridor USA Inc. and the FDA: common questions

Has Bridor USA Inc. received an FDA warning letter?

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

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

When did the FDA last inspect Bridor USA Inc.?

The most recent FDA inspection on file ended Jul 23, 2020 at Bridgeport, CT and was classified NAI. FDA has 5 inspections of Bridor USA Inc. on file.

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