Mizutamari Shokuhin Co., Ltd.
⚠️ Moderate Risk
FEI: 3013267376 • Minamisatsuma, Kagoshima • JAPAN
FEI Number
3013267376
Location
Minamisatsuma, Kagoshima
Country
JAPANAddress
2940 Miyazaki, Kinpou-chou, Minamisatsuma, Kagoshima, 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.
Refusal History
Frequently Asked Questions
What is Mizutamari Shokuhin Co., Ltd.'s FDA import refusal history?
Mizutamari Shokuhin Co., Ltd. (FEI: 3013267376) has 2 FDA import refusal record(s) in our database, spanning from 12/20/2011 to 12/20/2011.
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. Mizutamari Shokuhin Co., Ltd.'s FEI number is 3013267376.
What types of violations has Mizutamari Shokuhin Co., Ltd. received?
Mizutamari Shokuhin Co., Ltd. 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 Mizutamari Shokuhin Co., Ltd. come from?
All FDA import refusal data for Mizutamari Shokuhin Co., Ltd. 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.