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Kaneso 22 Co., Ltd.

FDA import alert and refusal historyKasaoka, JapanFEI 3004267114

Recorded by FDA as KANESO 22 CO., LTD.

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Example subjectKaneso 22 Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kaneso 22 Co., Ltd. is on the green list of FDA Import Alert 16-74, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Kaneso 22 Co., Ltd.

3 records, newest first. Each line links to the FDA page it came from.

2019

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2015

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2009

  1. Import alert listing
    Listed on Import Alert 16-74green listSardines (Brisling, Sprats, Pilchards, Etc.), Ntrl/Artfcl Dried; Product name - Ohba Dashi Iriko.
    Source

Questions about Kaneso 22 Co., Ltd.

Is Kaneso 22 Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Kaneso 22 Co., Ltd. is on the green list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for sardines (brisling, sprats, pilchards, etc.), ntrl/artfcl dried; product name - ohba dashi iriko.; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Kaneso 22 Co., Ltd.?
No FDA import refusals for Kaneso 22 Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Kaneso 22 Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Kaneso 22 Co., Ltd. with a final classification is dated February 8, 2019 and was classified VAI (Voluntary Action Indicated).
What is Kaneso 22 Co., Ltd.'s FEI number?
Kaneso 22 Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004267114.

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Example subjectKaneso 22 Co., Ltd 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.