SupplierRadar

Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai

FDA import alert and refusal historyAmakusa, JapanFEI 1000412469

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectKumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumia added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 27, 2026, Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai 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 Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai

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
    Source

Questions about Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai

Is Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai on an FDA import alert?
Yes. As of October 27, 2026, Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai 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; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai?
No FDA import refusals for Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai appear in FDA's refusal data since October 2016, as of October 27, 2026.
When was Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai last inspected by FDA?
FDA's most recent inspection of Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai with a final classification is dated October 27, 2009 and was classified VAI (Voluntary Action Indicated).
What is Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai's FEI number?
Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai's FDA Establishment Identifier (FEI) is 1000412469.

Buying from Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectKumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumia added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.