MARUTEN TSUKEMONO
⚠️ Moderate Risk
FEI: 3004252158 • HAMAMATSU SHI, JP-22 • JAPAN
FEI Number
3004252158
Location
HAMAMATSU SHI, JP-22
Country
JAPANAddress
4307-1 Ookubo-cho, , HAMAMATSU SHI, JP-22, Japan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/10/2011 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) | |
| 10/19/2010 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) | |
| 9/22/2010 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | 64YELLOW #5 | San Francisco District Office (SAN-DO) |
| 9/22/2010 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | 64YELLOW #5 | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is MARUTEN TSUKEMONO's FDA import refusal history?
MARUTEN TSUKEMONO (FEI: 3004252158) has 4 FDA import refusal record(s) in our database, spanning from 9/22/2010 to 1/10/2011.
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. MARUTEN TSUKEMONO's FEI number is 3004252158.
What types of violations has MARUTEN TSUKEMONO received?
MARUTEN TSUKEMONO has been cited for 3 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 MARUTEN TSUKEMONO come from?
All FDA import refusal data for MARUTEN TSUKEMONO 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.