Tomoni Alive
⚠️ Moderate Risk
FEI: 3011268628 • Toyohashi-shi, Aichi-ken • JAPAN
FEI Number
3011268628
Location
Toyohashi-shi, Aichi-ken
Country
JAPANAddress
218 Nakahamachi, , Toyohashi-shi, Aichi-ken, 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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
INCONSPICU
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
NCONTACTS
The product is a dietary supplement that is marketed in the United States and appears to not have a domestic address or domestic phone number through which the responsible person may receive a report of a serious adverse event.
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/25/2015 | 54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | Cincinnati District Office (CIN-DO) | |
| 2/25/2015 | 04CYY07NOODLES, INSTANT | 324NO ENGLISH | Cincinnati District Office (CIN-DO) |
| 2/25/2015 | 34FYY02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT | Cincinnati District Office (CIN-DO) | |
| 2/17/2015 | 24FYI20CUCUMBERS (FRUIT USED AS VEGETABLE) | 482NUTRIT LBL | Cincinnati District Office (CIN-DO) |
| 2/17/2015 | 34FYY02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT | 482NUTRIT LBL | Cincinnati District Office (CIN-DO) |
| 2/17/2015 | 33LYY05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 482NUTRIT LBL | Cincinnati District Office (CIN-DO) |
| 2/17/2015 | 03HYY02CHOCOLATE PLAIN COOKIES,BISCUITS AND WAFERS | Cincinnati District Office (CIN-DO) | |
| 2/17/2015 | 34FYY02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT | Cincinnati District Office (CIN-DO) | |
| 2/17/2015 | 33LYY05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Cincinnati District Office (CIN-DO) | |
| 2/6/2015 | 04CYY99NOODLES AND NOODLE PRODUCTS, N.E.C. | Cincinnati District Office (CIN-DO) | |
| 1/21/2015 | 53BY01BATH OILS, TABLETS AND SALTS (BATH PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 1/21/2015 | 04CYY07NOODLES, INSTANT | 256INCONSPICU | Cincinnati District Office (CIN-DO) |
| 1/20/2015 | 04BGH99EGG NOODLES, N.E.C. | Cincinnati District Office (CIN-DO) | |
| 1/20/2015 | 03YGY12RICE CAKES | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Tomoni Alive's FDA import refusal history?
Tomoni Alive (FEI: 3011268628) has 14 FDA import refusal record(s) in our database, spanning from 1/20/2015 to 2/25/2015.
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. Tomoni Alive's FEI number is 3011268628.
What types of violations has Tomoni Alive received?
Tomoni Alive has been cited for 7 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 Tomoni Alive come from?
All FDA import refusal data for Tomoni Alive 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.