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The Belport Company, Inc FDA Record

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

Latest inspection VAI · Nov 12, 2021
No warning letters matched by name

Inspections 4

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 2 Latest Feb 22, 1982

The Belport Company, Inc has 0 FDA recalls, 4 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "The Belport Company, Inc" is on file.

What these totals cover: FDA records filed under the name "The Belport Company, Inc" and its spelling variants "Belport Company", "Belport Co". Records filed under related names are not included; see Related names.

Latest inspection: Nov 12, 2021 · VAI
Latest 510(k): Feb 22, 1982

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	2	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

The Belport Company, Inc's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

The Belport Company, Inc: FDA inspections per year

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	1	0	0	0	0
2020	0	0	0	0	0
2019	1	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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Related names

Each name below has its own page. Its counts cover only the records FDA filed under that name and are not part of the totals for The Belport Company, Inc above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
Belport Company Inc., Dba Gingi-Pak	Same company group	0	1	0	0	—

Recent FDA inspections

4 inspections from Mar 14, 2012 to Nov 12, 2021.

Date	Site	Product	Classification	FEI
Nov 12, 2021	Camarillo, CA	Drugs	Voluntary Action Indicated (VAI)	2014676
Jan 23, 2019	Camarillo, CA	Devices	No Action Indicated (NAI)	2014676
Sep 30, 2014	Camarillo, CA	Devices	No Action Indicated (NAI)	2014676
Mar 14, 2012	Camarillo, CA	Devices	Voluntary Action Indicated (VAI)	2014676

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 2014676	Camarillo, CA	4	Nov 12, 2021

Recent 510(k) clearances

2 510(k) clearances from Sep 8, 1981 to Feb 22, 1982.

K-Number	Device	Date
K820061	REVERSIBLE HYDROCOLLOID IMPRESSION MAT	Feb 22, 1982
K812120	GINGI-PLAIN CORDS & BRAIDS	Sep 8, 1981

The Belport Company, Inc and the FDA: common questions

Has The Belport Company, Inc received an FDA warning letter?

No FDA warning letter addressed to the name "The Belport Company, 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 The Belport Company, Inc received an FDA Form 483?

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

When did the FDA last inspect The Belport Company, Inc?

The most recent FDA inspection on file ended Nov 12, 2021 at Camarillo, CA and was classified VAI. FDA has 4 inspections of The Belport Company, Inc on file.

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