Izumiya Confectionary Co., Ltd.
⚠️ Moderate Risk
FEI: 1000341856 • Toshima • JAPAN
FEI Number
1000341856
Location
Toshima
Country
JAPANAddress
Shippo-Cho, Ama-Gun, Aichi, 90; Totsubo, Toshima, , 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 Izumiya Confectionary Co., Ltd.'s FDA import refusal history?
Izumiya Confectionary Co., Ltd. (FEI: 1000341856) has 2 FDA import refusal record(s) in our database, spanning from 8/22/2012 to 8/22/2012.
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. Izumiya Confectionary Co., Ltd.'s FEI number is 1000341856.
What types of violations has Izumiya Confectionary Co., Ltd. received?
Izumiya Confectionary 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 Izumiya Confectionary Co., Ltd. come from?
All FDA import refusal data for Izumiya Confectionary 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.