Nippon Suisan Kaisha Ltd
✅ Low Risk
FEI: 3002712675 • Chiyoda, Tokyo • JAPAN
FEI Number
3002712675
Location
Chiyoda, Tokyo
Country
JAPANAddress
2 Chome 6-2 Nippon Bldg. 10f, Ote-Machi, Chiyoda, Tokyo, Japan
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
FALSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
Frequently Asked Questions
What is Nippon Suisan Kaisha Ltd's FDA import refusal history?
Nippon Suisan Kaisha Ltd (FEI: 3002712675) has 1 FDA import refusal record(s) in our database, spanning from 3/9/2007 to 3/9/2007.
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. Nippon Suisan Kaisha Ltd's FEI number is 3002712675.
What types of violations has Nippon Suisan Kaisha Ltd received?
Nippon Suisan Kaisha Ltd has been cited for 2 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 Nippon Suisan Kaisha Ltd come from?
All FDA import refusal data for Nippon Suisan Kaisha 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.