Maruei Suisan Co.,Ltd.
FDA import alert and refusal historyMonbetsu, JapanFEI 3012772392
Recorded by FDA as MARUEI SUISAN CO.,LTD.
As of October 26, 2026, Maruei Suisan Co.,Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 23, 2025, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Scallops, aquaculture harvested fishery/seafood products · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Maruei Suisan Co.,Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Scallops, aquaculture harvested fishery/seafood productsFILTHYEntry KM6-1621246-0Show 2 linesHide lines
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Maruei Suisan Co.,Ltd.
- Is Maruei Suisan Co.,Ltd. on an FDA import alert?
- No listing for Maruei Suisan Co.,Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Maruei Suisan Co.,Ltd.?
- Yes. FDA refused 2 shipment lines from Maruei Suisan Co.,Ltd. on January 23, 2025. The most recent, on January 23, 2025, was scallops, aquaculture harvested fishery/seafood products, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Maruei Suisan Co.,Ltd.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Maruei Suisan Co.,Ltd.'s FEI number?
- Maruei Suisan Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3012772392.
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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.