KAGAWAKEN GYOREN
⚠️ Moderate Risk
FEI: 3004308382 • Marugame, Kagawa • JAPAN
FEI Number
3004308382
Location
Marugame, Kagawa
Country
JAPANAddress
28-11, Horai-Cho, Marugame, Kagawa, 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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
Frequently Asked Questions
What is KAGAWAKEN GYOREN's FDA import refusal history?
KAGAWAKEN GYOREN (FEI: 3004308382) has 2 FDA import refusal record(s) in our database, spanning from 3/20/2013 to 3/20/2013.
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. KAGAWAKEN GYOREN's FEI number is 3004308382.
What types of violations has KAGAWAKEN GYOREN received?
KAGAWAKEN GYOREN 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 KAGAWAKEN GYOREN come from?
All FDA import refusal data for KAGAWAKEN GYOREN 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.