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Cayman Chemical Company, Inc. FDA Record

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

Cayman Chemical Company, Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Cayman Chemical Company, Inc., the most recent on Jan 19, 2010.

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

Latest inspection: Apr 17, 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	7	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

Cayman Chemical Company, 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	0	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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Cayman Chemical Company, Inc. FDA Warning Letters

1 warning letter on Jan 19, 2010.

Issued	Subject	Issuing office	Close-out letter
Jan 19, 2010

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

7 inspections from May 18, 2009 to Apr 17, 2025.

Date	Site	Product	Classification	FEI
Apr 17, 2025	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
Dec 3, 2018	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
Nov 19, 2014	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
Feb 28, 2013	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
Dec 22, 2011	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
Dec 15, 2010	Ann Arbor, MI	Drugs	Voluntary Action Indicated (VAI)	3002715502
May 18, 2009	Ann Arbor, MI	Drugs	Official Action Indicated (OAI)	3002715502

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 Cayman Chemical Company, Inc.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jan 19, 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 3002715502	Ann Arbor, MI	7	Apr 17, 2025

Cayman Chemical Company, Inc. and the FDA: common questions

Has Cayman Chemical Company, Inc. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Cayman Chemical Company, Inc.. The most recent is dated Jan 19, 2010.

Has Cayman Chemical Company, Inc. received an FDA Form 483?

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

When did the FDA last inspect Cayman Chemical Company, Inc.?

The most recent FDA inspection on file ended Apr 17, 2025 at Ann Arbor, MI and was classified VAI. FDA has 7 inspections of Cayman Chemical Company, Inc. on file, 1 of them classified OAI (official action indicated).

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