KIRISHIMA NOUSAN CO.,LTD.
⚠️ Moderate Risk
FEI: 3004251579 • Kobayashi, Miyazaki • JAPAN
FEI Number
3004251579
Location
Kobayashi, Miyazaki
Country
JAPANAddress
734-120, Kitanishikata, Kobayashi, Miyazaki, 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).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/6/2021 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | Division of West Coast Imports (DWCI) | |
| 12/6/2021 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | Division of West Coast Imports (DWCI) | |
| 4/19/2012 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) | |
| 10/19/2010 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is KIRISHIMA NOUSAN CO.,LTD.'s FDA import refusal history?
KIRISHIMA NOUSAN CO.,LTD. (FEI: 3004251579) has 4 FDA import refusal record(s) in our database, spanning from 10/19/2010 to 12/6/2021.
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. KIRISHIMA NOUSAN CO.,LTD.'s FEI number is 3004251579.
What types of violations has KIRISHIMA NOUSAN CO.,LTD. received?
KIRISHIMA NOUSAN CO.,LTD. has been cited for 3 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 KIRISHIMA NOUSAN CO.,LTD. come from?
All FDA import refusal data for KIRISHIMA NOUSAN 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.