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Takeda Yakuhin Kogyo Co Ltd

FDA import alert and refusal historyChuo, JapanFEI 3003913982

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Example subjectTakeda Yakuhin Kogyo Co Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Takeda Yakuhin Kogyo Co Ltd (Chuo, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink house c 1000 lemon water, published by FDA on October 12, 2011, 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 Takeda Yakuhin Kogyo Co Ltd

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

2011

  1. Import alert listing
    Listed on Import Alert 45-02red listSoft Drink House C 1000 Lemon Water
    Source

Questions about Takeda Yakuhin Kogyo Co Ltd

Is Takeda Yakuhin Kogyo Co Ltd on an FDA import alert?
Yes. As of October 26, 2026, Takeda Yakuhin Kogyo Co Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink house c 1000 lemon water; FDA published the listing on October 12, 2011.
Has FDA refused shipments from Takeda Yakuhin Kogyo Co Ltd?
No FDA import refusals for Takeda Yakuhin Kogyo Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Takeda Yakuhin Kogyo Co Ltd's FEI number?
Takeda Yakuhin Kogyo Co Ltd's FDA Establishment Identifier (FEI) is 3003913982.
Can shipments from Takeda Yakuhin Kogyo Co Ltd still enter the U.S.?
Shipments of soft drink house c 1000 lemon water from Takeda Yakuhin Kogyo 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 subjectTakeda Yakuhin Kogyo Co Lt 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.