Rangen, LLC FDA Record

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

Rangen, LLC has 0 FDA recalls, 39 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Rangen, LLC, the most recent on Feb 16, 2010.

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

Latest inspection
Dec 18, 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
Inspections39Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Rangen, LLC: FDA inspections per year 2017: 4 inspections420172018: 5 inspections520182019: 2 inspections220192020: 0 inspections020202021: 1 inspections120212022: 1 inspections120222023: 2 inspections220232024: 2 inspections220242025: 2 inspections220252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202520000
202420000
202320000
202210000
202110000
202000000
201920000
201850000
201740000

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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Rangen, LLC FDA Warning Letters

1 warning letter on Feb 16, 2010.

IssuedSubjectIssuing officeClose-out letter
Feb 16, 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

39 inspections from Nov 10, 2008 to Dec 18, 2025. Showing the 20 most recent. View all 39 inspections

DateSiteProductClassificationFEI
Dec 18, 2025El Centro, CAVeterinaryNo Action Indicated (NAI)3010022658
Mar 26, 2025Rosser, TXVeterinaryNo Action Indicated (NAI)3008933487
Jul 9, 2024Idaho Falls, IDVeterinaryNo Action Indicated (NAI)3007757641
Jan 26, 2024Clackamas, ORVeterinaryVoluntary Action Indicated (VAI)3011649
Dec 7, 2023Buhl, IDVeterinaryNo Action Indicated (NAI)3016448
Aug 16, 2023Cincinnati, OHVeterinaryVoluntary Action Indicated (VAI)1511961
Mar 23, 2022El Centro, CAVeterinaryNo Action Indicated (NAI)3010022658
Jul 29, 2021Buhl, IDVeterinaryNo Action Indicated (NAI)3016448
Oct 29, 2019Saint Joseph, MOVeterinaryNo Action Indicated (NAI)1916160
Aug 1, 2019Ogden, UTVeterinaryNo Action Indicated (NAI)1714764
Sep 20, 2018Angleton, TXVeterinaryNo Action Indicated (NAI)1000149809
May 22, 2018Clackamas, ORVeterinaryNo Action Indicated (NAI)3011649
Mar 1, 2018Buhl, IDVeterinaryVoluntary Action Indicated (VAI)3016448
Jan 9, 2018Saint Joseph, MOVeterinaryNo Action Indicated (NAI)1931382
Jan 9, 2018Saint Joseph, MOVeterinaryNo Action Indicated (NAI)1916160
Dec 19, 2017Cincinnati, OHVeterinaryNo Action Indicated (NAI)1511961
Aug 30, 2017Ogden, UTVeterinaryNo Action Indicated (NAI)1714764
May 22, 2017Saint Joseph, MOVeterinaryNo Action Indicated (NAI)1931382
Mar 27, 2017Rosser, TXVeterinaryNo Action Indicated (NAI)3008933487
Mar 5, 2015Saint Joseph, MOVeterinaryVoluntary Action Indicated (VAI)1931382
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 Rangen, LLC: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Feb 16, 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

10 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3010022658El Centro, CA2Dec 18, 2025
FEI 3008933487Rosser, TX3Mar 26, 2025
FEI 3007757641Idaho Falls, ID1Jul 9, 2024
FEI 3011649Clackamas, OR4Jan 26, 2024
FEI 3016448Buhl, ID7Dec 7, 2023
FEI 1511961Cincinnati, OH3Aug 16, 2023
FEI 1916160Saint Joseph, MO4Oct 29, 2019
FEI 1714764Ogden, UT4Aug 1, 2019
FEI 1000149809Angleton, TX3Sep 20, 2018
FEI 1931382Saint Joseph, MO8Jan 9, 2018

Rangen, LLC and the FDA: common questions

Has Rangen, LLC received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Rangen, LLC. The most recent is dated Feb 16, 2010.

Has Rangen, LLC received an FDA Form 483?

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

When did the FDA last inspect Rangen, LLC?

The most recent FDA inspection on file ended Dec 18, 2025 at El Centro, CA and was classified NAI. FDA has 39 inspections of Rangen, LLC on file, 1 of them classified OAI (official action indicated).

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