Marutomo
⚠️ High Risk
FEI: 3009923966 • Iyo, Ehime • JAPAN
FEI Number
3009923966
Location
Iyo, Ehime
Country
JAPANAddress
Azamachida Child Iyo Plant 53-1, Hongu, Iyo, Ehime, Japan
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/14/2009 | 16MGT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 1/14/2009 | 16MGT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 1/14/2009 | 16MGT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 7/31/2008 | 16MHT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 7/31/2008 | 16MHT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 5/7/2007 | 16MGT03SQUID, OTHER AQUATIC SPECIES | 295LISTERIA | Atlanta District Office (ATL-DO) |
| 4/6/2007 | 16MGT07CUTTLEFISH, OTHER AQUATIC SPECIES | 295LISTERIA | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Marutomo's FDA import refusal history?
Marutomo (FEI: 3009923966) has 7 FDA import refusal record(s) in our database, spanning from 4/6/2007 to 1/14/2009.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Marutomo's FEI number is 3009923966.
What types of violations has Marutomo received?
Marutomo has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Marutomo come from?
All FDA import refusal data for Marutomo is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.