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Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory

FDA import alert and refusal historyIzumi-Gun, JapanFEI 3001448949

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Example subjectAzuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory 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

Import alerts
IA 16-125 · green list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory

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

2014

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2011

  1. Import alert listing
    Listed on Import Alert 16-125green listVacuum Packed Yellowtail (Tuna)
    Source

2009

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Questions about Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory

Is Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory on an FDA import alert?
Yes. As of October 26, 2026, Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for vacuum packed yellowtail (tuna); FDA published the listing on July 7, 2011.
Has FDA refused shipments from Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory?
No FDA import refusals for Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory last inspected by FDA?
FDA's most recent inspection of Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory with a final classification is dated February 18, 2014 and was classified VAI (Voluntary Action Indicated).
What is Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory's FEI number?
Azuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factory's FDA Establishment Identifier (FEI) is 3001448949.

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Example subjectAzuma-cho Gyogyo Kyodo Kumiai Marine Products Processing Factor 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.