Yugen Kaisha Yamamoto Shoji
FDA import alert and refusal historyKobe, JapanFEI 3012846272
As of October 26, 2026, Yugen Kaisha Yamamoto Shoji (Kobe, Japan) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for anchovy, published by FDA on September 10, 2009, is also listed on Import Alert 16-74 (green list), 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 16-74 · green listIA 16-119 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Yugen Kaisha Yamamoto Shoji
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-74green listDried Kaeri Anchovy/Ohba Kaeti AnchovySource
- Import alert listingListed on Import Alert 16-119red listAnchovySource
Questions about Yugen Kaisha Yamamoto Shoji
- Is Yugen Kaisha Yamamoto Shoji on an FDA import alert?
- Yes. As of October 26, 2026, Yugen Kaisha Yamamoto Shoji is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for anchovy; FDA published the listing on September 10, 2009.
- Has FDA refused shipments from Yugen Kaisha Yamamoto Shoji?
- No FDA import refusals for Yugen Kaisha Yamamoto Shoji appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Yugen Kaisha Yamamoto Shoji's FEI number?
- Yugen Kaisha Yamamoto Shoji's FDA Establishment Identifier (FEI) is 3012846272.
- Can shipments from Yugen Kaisha Yamamoto Shoji still enter the U.S.?
- Shipments of anchovy from Yugen Kaisha Yamamoto Shoji can be detained without physical examination under Import Alert 16-119; 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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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.