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TANSEIDO HOMPO

⚠️ Moderate Risk

FEI: 3011634543 • Osaka, Osaka • JAPAN

FEI

FEI Number

3011634543

📍

Location

Osaka, Osaka

🇯🇵

Country

JAPAN
🏢

Address

1 Chome 4-15 Shin'Imazato, Ikuno; Shin'Imazato; Ikuno, Osaka, Osaka, Japan

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
7/15/2024
Latest Refusal
8/15/2023
Earliest Refusal

Score Breakdown

Violation Severity
35.7×40%
Refusal Volume
22.3×30%
Recency
55.3×20%
Frequency
30.0×10%
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

3243×

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)).

2182×

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.

4822×

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.

Refusal History

DateProductViolationsDivision
7/15/2024
33LYT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Division of Southeast Imports (DSEI)
8/15/2023
33LYT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
8/15/2023
33SYT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TANSEIDO HOMPO's FDA import refusal history?

TANSEIDO HOMPO (FEI: 3011634543) has 3 FDA import refusal record(s) in our database, spanning from 8/15/2023 to 7/15/2024.

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. TANSEIDO HOMPO's FEI number is 3011634543.

What types of violations has TANSEIDO HOMPO received?

TANSEIDO HOMPO 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 TANSEIDO HOMPO come from?

All FDA import refusal data for TANSEIDO HOMPO 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.