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Samho Company Ltd

⚠️ Moderate Risk

FEI: 1000131717 • Seoul • SOUTH KOREA

FEI

FEI Number

1000131717

📍

Location

Seoul

🇰🇷
🏢

Address

2756 Yangjae Dong, , Seoul, , South Korea

Moderate Risk

FDA Import Risk Assessment

26.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
4/7/2010
Latest Refusal
5/14/2007
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
10.3×10%
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

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.

3242×

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)).

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
4/7/2010
16RGT02CRAB, IMITATION
218LIST INGRE
324NO ENGLISH
Los Angeles District Office (LOS-DO)
4/7/2010
16RGT02CRAB, IMITATION
218LIST INGRE
324NO ENGLISH
Los Angeles District Office (LOS-DO)
5/14/2007
16AGT56FILEFISH
9SALMONELLA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Samho Company Ltd's FDA import refusal history?

Samho Company Ltd (FEI: 1000131717) has 3 FDA import refusal record(s) in our database, spanning from 5/14/2007 to 4/7/2010.

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. Samho Company Ltd's FEI number is 1000131717.

What types of violations has Samho Company Ltd received?

Samho Company 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 Samho Company Ltd come from?

All FDA import refusal data for Samho Company 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.