Suntory Co Ltd
⚠️ Moderate Risk
FEI: 3004903523 • Kyoto, Kyoto • JAPAN
FEI Number
3004903523
Location
Kyoto, Kyoto
Country
JAPANAddress
80 Tominoara, Ida-Cho; Kamigyo, Kyoto, Kyoto, 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
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/12/2011 | 29YGY99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | 11UNSAFE COL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Suntory Co Ltd's FDA import refusal history?
Suntory Co Ltd (FEI: 3004903523) has 1 FDA import refusal record(s) in our database, spanning from 7/12/2011 to 7/12/2011.
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. Suntory Co Ltd's FEI number is 3004903523.
What types of violations has Suntory Co Ltd received?
Suntory 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 Suntory Co Ltd come from?
All FDA import refusal data for Suntory 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.