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Yamashinaya Seika Co., Ltd.

FDA import alert and refusal historyNagoya, JapanFEI 3004299888

Recorded by FDA as YAMASHINAYA SEIKA CO., LTD.

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

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As of October 26, 2026, Yamashinaya Seika Co., Ltd. (Nagoya, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for rice cakes, published by FDA on September 18, 2009, 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 Yamashinaya Seika Co., Ltd.

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listRice Cakes
    Source

Questions about Yamashinaya Seika Co., Ltd.

Is Yamashinaya Seika Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Yamashinaya Seika Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for rice cakes; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Yamashinaya Seika Co., Ltd.?
No FDA import refusals for Yamashinaya Seika Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Yamashinaya Seika Co., Ltd.'s FEI number?
Yamashinaya Seika Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004299888.
Can shipments from Yamashinaya Seika Co., Ltd. still enter the U.S.?
Shipments of rice cakes from Yamashinaya Seika 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 subjectYamashinaya Seika 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.