KIMURA TUKEMONO MIYAZAKI CO.,LTD
⚠️ Moderate Risk
FEI: 3004248334 • GOTOU GUN, JP-45 • JAPAN
FEI Number
3004248334
Location
GOTOU GUN, JP-45
Country
JAPANAddress
8935 Kami Tomita Shin Tomita, , GOTOU GUN, JP-45, 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).
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.
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
Frequently Asked Questions
What is KIMURA TUKEMONO MIYAZAKI CO.,LTD's FDA import refusal history?
KIMURA TUKEMONO MIYAZAKI CO.,LTD (FEI: 3004248334) has 1 FDA import refusal record(s) in our database, spanning from 3/7/2008 to 3/7/2008.
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. KIMURA TUKEMONO MIYAZAKI CO.,LTD's FEI number is 3004248334.
What types of violations has KIMURA TUKEMONO MIYAZAKI CO.,LTD received?
KIMURA TUKEMONO MIYAZAKI 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 KIMURA TUKEMONO MIYAZAKI CO.,LTD come from?
All FDA import refusal data for KIMURA TUKEMONO MIYAZAKI 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.