Marutomo Co., Ltd.
FDA import alert and refusal historyIyo, JapanFEI 3004257555
Recorded by FDA as MARUTOMO CO., LTD.
As of October 25, 2026, Marutomo Co., Ltd. (Iyo, Japan) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for fish roe, fishery products, n.e.c., published by FDA on September 18, 2009, 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 16-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Marutomo 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 16-39red listFish Roe, Fishery Products, n.e.c.Source
Questions about Marutomo Co., Ltd.
- Is Marutomo Co., Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, Marutomo Co., Ltd. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for fish roe, fishery products, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Marutomo Co., Ltd.?
- No FDA import refusals for Marutomo Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Marutomo Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Marutomo Co., Ltd. with a final classification is dated December 8, 2009 and was classified VAI (Voluntary Action Indicated).
- What is Marutomo Co., Ltd.'s FEI number?
- Marutomo Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004257555.
- Can shipments from Marutomo Co., Ltd. still enter the U.S.?
- Shipments of fish roe, fishery products, n.e.c. from Marutomo Co., Ltd. can be detained without physical examination under Import Alert 16-39; 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.