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Azuma Foods Co. Ltd.

FDA import alert and refusal historyYokkaichi, JapanFEI 1000431466

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Example subjectAzuma Foods Co. Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Azuma Foods Co. Ltd. (Yokkaichi, Japan) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for squid, other aquatic species; seasoned cuttlefish, published by FDA on March 13, 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 Azuma Foods 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 16-39red listSquid, Other Aquatic Species; Seasoned cuttlefish
    Source

Questions about Azuma Foods Co. Ltd.

Is Azuma Foods Co. Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Azuma Foods Co. Ltd. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for squid, other aquatic species; seasoned cuttlefish; FDA published the listing on March 13, 2009.
Has FDA refused shipments from Azuma Foods Co. Ltd.?
No FDA import refusals for Azuma Foods Co. Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Azuma Foods Co. Ltd.'s FEI number?
Azuma Foods Co. Ltd.'s FDA Establishment Identifier (FEI) is 1000431466.
Can shipments from Azuma Foods Co. Ltd. still enter the U.S.?
Shipments of squid, other aquatic species; seasoned cuttlefish from Azuma Foods Co. Ltd. can be detained without physical examination under Import Alert 16-39; 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 subjectAzuma Foods 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.