KINOKOMURA
⚠️ High Risk
FEI: 3014336506 • Suzaka, Nagano • JAPAN
FEI Number
3014336506
Location
Suzaka, Nagano
Country
JAPANAddress
931, Kamekura-Machi, Suzaka, Nagano, 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
Frequently Asked Questions
What is KINOKOMURA's FDA import refusal history?
KINOKOMURA (FEI: 3014336506) has 3 FDA import refusal record(s) in our database, spanning from 5/17/2022 to 5/19/2023.
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. KINOKOMURA's FEI number is 3014336506.
What types of violations has KINOKOMURA received?
KINOKOMURA 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 KINOKOMURA come from?
All FDA import refusal data for KINOKOMURA 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.