Hyoshoku Co., Ltd.
FDA import alert and refusal historyTsukumi, JapanFEI 3010013024
Recorded by FDA as HYOSHOKU CO., LTD.
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
- 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 Hyoshoku Co., Ltd.
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 Packaging, Raw, Fresh, RefrigeratedSource
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.
Buying from Hyoshoku Co., Ltd.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.