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Yamatake Shyokuhin Co., Ltd.

FDA import alert and refusal historyMie-Gun, JapanFEI 3004319584

Recorded by FDA as YAMATAKE SHYOKUHIN CO., LTD.

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

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As of October 26, 2026, Yamatake Shyokuhin Co., Ltd. (Mie-Gun, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for chu chu bars, published by FDA on May 8, 2014, 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
None on record

Every FDA record for Yamatake Shyokuhin Co., Ltd.

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

2014

  1. Import alert listing
    Listed on Import Alert 45-02red listChu Chu Bars
    Source

Questions about Yamatake Shyokuhin Co., Ltd.

Is Yamatake Shyokuhin Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Yamatake Shyokuhin Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chu chu bars; FDA published the listing on May 8, 2014.
Has FDA refused shipments from Yamatake Shyokuhin Co., Ltd.?
No FDA import refusals for Yamatake Shyokuhin Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Yamatake Shyokuhin Co., Ltd.'s FEI number?
Yamatake Shyokuhin Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004319584.
Can shipments from Yamatake Shyokuhin Co., Ltd. still enter the U.S.?
Shipments of chu chu bars from Yamatake Shyokuhin Co., Ltd. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectYamatake Shyokuhin 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.