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Kohyo Co., Ltd.

FDA import alert and refusal historyYokkaichi, JapanFEI 3004324486

Recorded by FDA as KOHYO CO., LTD.

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

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As of October 25, 2026, Kohyo Co., Ltd. (Yokkaichi, Japan) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for saury, published by FDA on January 16, 2015, is also listed on Import Alert 45-02 (red list), and has 7 FDA import refusals recorded since October 2016.

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

Current status

Import alerts
IA 16-119 · red listIA 45-02 · red list
Last import refusal
Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Kohyo Co., Ltd.

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

2019

  1. Import refusal
    Refused, 7 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.); Carbonated soft drink, n.e.c. and 2 moreNO ENGLISHEntry DR7-0080035-9Show 7 lines
    Source

2015

  1. Import alert listing
    Listed on Import Alert 16-119red listSaury
    Source

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listcapelin roe
    Source

Refusal charges, in plain English

  • NO ENGLISH7 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Kohyo Co., Ltd.

Is Kohyo Co., Ltd. on an FDA import alert?
Yes. As of October 25, 2026, Kohyo Co., Ltd. is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for saury; FDA published the listing on January 16, 2015.
Has FDA refused shipments from Kohyo Co., Ltd.?
Yes. FDA refused 7 shipment lines from Kohyo Co., Ltd. on December 27, 2019. The most recent, on December 27, 2019, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Kohyo Co., Ltd.'s shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 7 lines).
What is Kohyo Co., Ltd.'s FEI number?
Kohyo Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004324486.
Can shipments from Kohyo Co., Ltd. still enter the U.S.?
Shipments of saury from Kohyo Co., Ltd. can be detained without physical examination under Import Alert 16-119; 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 subjectKohyo 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.