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Hyoshoku Co., Ltd.

FDA import alert and refusal historyTsukumi, JapanFEI 3010013024

Recorded by FDA as HYOSHOKU CO., LTD.

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

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As of October 25, 2026, Hyoshoku Co., Ltd. is on the green list of FDA Import Alert 16-125, 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 Hyoshoku Co., Ltd.

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

2009

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source
  2. Import alert listing
    Listed on Import Alert 16-125green listYellowtail, Amberjack, Vacuum or Modified Atmosphere Packaging, Raw, Fresh, Refrigerated
    Source

Questions about Hyoshoku Co., Ltd.

Is Hyoshoku Co., Ltd. on an FDA import alert?
Yes. As of October 25, 2026, Hyoshoku Co., Ltd. is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for yellowtail, amberjack, vacuum or modified atmosphere packaging, raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Hyoshoku Co., Ltd.?
No FDA import refusals for Hyoshoku Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Hyoshoku Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Hyoshoku Co., Ltd. with a final classification is dated November 3, 2009 and was classified VAI (Voluntary Action Indicated).
What is Hyoshoku Co., Ltd.'s FEI number?
Hyoshoku Co., Ltd.'s FDA Establishment Identifier (FEI) is 3010013024.

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Example subjectHyoshoku 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.