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Catalina Offshore Products, Inc FDA Record

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

Catalina Offshore Products, Inc has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Catalina Offshore Products, Inc, the most recent on Jun 14, 2010.

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

Latest inspection: Jul 21, 2025 · VAI

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	8	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Catalina Offshore Products, 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	1	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	1	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	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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Catalina Offshore Products, Inc FDA Warning Letters

1 warning letter on Jun 14, 2010.

Issued	Subject	Issuing office	Close-out letter
Jun 14, 2010 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

8 inspections from Apr 9, 2010 to Jul 21, 2025.

Date	Site	Product	Classification	FEI
Jul 21, 2025	San Diego, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3000204855
Mar 16, 2022	San Diego, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3000204855
Aug 9, 2019	San Diego, CA	Food/Cosmetics	No Action Indicated (NAI)	3000204855
Aug 16, 2016	San Diego, CA	Food/Cosmetics	No Action Indicated (NAI)	3000204855
Sep 22, 2014	San Diego, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3000204855
Nov 25, 2013	San Diego, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3000204855
Dec 15, 2010	San Diego, CA	Food/Cosmetics	Voluntary Action Indicated (VAI)	3000204855
Apr 9, 2010	San Diego, CA	Food/Cosmetics	Official Action Indicated (OAI)	3000204855

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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Catalina Offshore Products, Inc: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jun 14, 2010.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3000204855	San Diego, CA	8	Jul 21, 2025

Catalina Offshore Products, Inc and the FDA: common questions

Has Catalina Offshore Products, Inc received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Catalina Offshore Products, Inc. The most recent is dated Jun 14, 2010.

Has Catalina Offshore Products, Inc received an FDA Form 483?

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

When did the FDA last inspect Catalina Offshore Products, Inc?

The most recent FDA inspection on file ended Jul 21, 2025 at San Diego, CA and was classified VAI. FDA has 8 inspections of Catalina Offshore Products, Inc on file, 1 of them classified OAI (official action indicated).

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