Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai
FDA import alert and refusal historyAmakusa, JapanFEI 1000412469
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
- 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 Kumamoto-Ken Kaisui Yoshoku Gyogyo Kyodo Kumiai
2 records, newest first. Each line links to the FDA page it came from.
2009
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 16-125green listYellowtail, Amberjack, Vacuum or Modified Atmosphere PackagingSource
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.
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