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Tomoni Alive

⚠️ Moderate Risk

FEI: 3010925593 • Toyohashi, Aichi • JAPAN

FEI

FEI Number

3010925593

📍

Location

Toyohashi, Aichi

🇯🇵

Country

JAPAN
🏢

Address

406-218 Haitsunakahama, Nakahama-Cho, Toyohashi, Aichi, Japan

Moderate Risk

FDA Import Risk Assessment

28.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

6
Total Refusals
2
Unique Violations
12/19/2014
Latest Refusal
10/29/2014
Earliest Refusal

Score Breakdown

Violation Severity
33.3×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

2564×

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)).

4712×

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.

Refusal History

DateProductViolationsDivision
12/19/2014
20KYY01CITRON, CITRUS FRUIT JUICES OR CONCENTRATES
256INCONSPICU
Cincinnati District Office (CIN-DO)
12/19/2014
20HYY01CITRON, DRIED OR PASTE
256INCONSPICU
Cincinnati District Office (CIN-DO)
12/19/2014
31NYY04KOHYANG YULMUCH TEA (ADLAY FLOUR, SOYBEAN POWDER, BARLEY FLOUR)
256INCONSPICU
Cincinnati District Office (CIN-DO)
12/19/2014
28AYY08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE)
256INCONSPICU
Cincinnati District Office (CIN-DO)
10/29/2014
53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Cincinnati District Office (CIN-DO)
10/29/2014
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Tomoni Alive's FDA import refusal history?

Tomoni Alive (FEI: 3010925593) has 6 FDA import refusal record(s) in our database, spanning from 10/29/2014 to 12/19/2014.

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 3010925593.

What types of violations has Tomoni Alive received?

Tomoni Alive 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 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.