Stellar Distributing

FDA Regulatory Profile

Stellar Distributing has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Stellar Distributing".

Latest inspection
Jul 10, 2026 · VAI

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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 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA Record by Year

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

Stellar Distributing: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 2 inspections220232024: 0 inspections020242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202400000
202320000
202200000
202100000
202000000
201900000
201800000
201700000

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.

Recent FDA Inspections

4 inspections from Jul 13, 2015 to Jul 10, 2026.

DateSiteProductClassificationFEI
Jul 10, 2026Madera, CAFood/CosmeticsVoluntary Action Indicated (VAI)3014670960
Sep 13, 2023Madera, CAFood/CosmeticsNo Action Indicated (NAI)3004248383
Jul 18, 2023Madera, CAFood/CosmeticsNo Action Indicated (NAI)3014670960
Jul 13, 2015Madera, CAVeterinaryNo Action Indicated (NAI)3004248383

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means 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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3014670960Madera, CA2Jul 10, 2026
FEI 3004248383Madera, CA2Sep 13, 2023

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