Cheyenne International, LLC FDA Record

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

Cheyenne International, LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Cheyenne International, LLC, the most recent on Dec 9, 2016.

What these totals cover: FDA records filed under the name "Cheyenne International, LLC" and its spelling variant "Cheyenne International".

Latest inspection
Apr 3, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

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Cheyenne International, LLC FDA Warning Letters

1 warning letter on Dec 9, 2016.

IssuedSubjectIssuing officeClose-out letter
Dec 9, 2016

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

4 inspections from Oct 13, 2011 to Apr 3, 2025.

DateSiteProductClassificationFEI
Apr 3, 2025Grover, NCTobaccoNo Action Indicated (NAI)3008255547
Jun 7, 2016Grover, NCTobaccoVoluntary Action Indicated (VAI)3008255547
Aug 7, 2014Grover, NCTobaccoNo Action Indicated (NAI)3008255547
Oct 13, 2011Grover, NCTobaccoNo Action Indicated (NAI)3008255547
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 Cheyenne International, LLC: warning letters, injunctions and seizures. It came from FDA's Center for Tobacco Products, which regulates tobacco retailers and manufacturers. It is not a drug, medical device or food manufacturing action.

Most recent: Warning Letter, Dec 9, 2016.

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.

FacilityLocationInspectionsLatest
FEI 3008255547Grover, NC4Apr 3, 2025

Cheyenne International, LLC and the FDA: common questions

Has Cheyenne International, LLC received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Cheyenne International, LLC. The most recent is dated Dec 9, 2016.

Has Cheyenne International, LLC received an FDA Form 483?

FDA has not published a Form 483 for "Cheyenne International, LLC" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Cheyenne International, LLC?

The most recent FDA inspection on file ended Apr 3, 2025 at Grover, NC and was classified NAI. FDA has 4 inspections of Cheyenne International, LLC on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.