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Kabizu Business Group

FDA import alert and refusal historyKigali, RwandaFEI 3018642682

Recorded by FDA as KABIZU BUSINESS GROUP

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Example subjectKabizu Business Grou added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kabizu Business Group is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 18, 2022, most often for filthy, putrid or decomposed substance (FILTHY).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Corn, bolted meal or flour · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Kabizu Business Group

1 record, newest first. Each line links to the FDA page it came from.

2022

  1. Import refusal
    Refused, Corn, bolted meal or flourFILTHYEntry BNI-0108969-5
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Kabizu Business Group

Is Kabizu Business Group on an FDA import alert?
No listing for Kabizu Business Group appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Rwanda page.
Has FDA refused shipments from Kabizu Business Group?
Yes. FDA refused 1 shipment line from Kabizu Business Group on August 18, 2022. The most recent, on August 18, 2022, was corn, bolted meal or flour, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Kabizu Business Group's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Kabizu Business Group's FEI number?
Kabizu Business Group's FDA Establishment Identifier (FEI) is 3018642682.

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Example subjectKabizu Business Grou added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.