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Daehan Red Ginseng Promotion Corporation

✅ Low Risk

FEI: 3010187121 • Geumsan-Gun, CHUNGNAM • SOUTH KOREA

FEI

FEI Number

3010187121

📍

Location

Geumsan-Gun, CHUNGNAM

🇰🇷
🏢

Address

392-1, Pacho-Ri, Geumseong-Myeon, , Geumsan-Gun, CHUNGNAM, South Korea

Low Risk

FDA Import Risk Assessment

24.8
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

4
Total Refusals
6
Unique Violations
2/8/2019
Latest Refusal
3/6/2017
Earliest Refusal

Score Breakdown

Violation Severity
37.5×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
20.7×10%
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

4824×

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.

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2562×

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)).

23001×

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.

3241×

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)).

38641×

NCONTACT

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(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

Refusal History

DateProductViolationsDivision
2/8/2019
54FYT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
256INCONSPICU
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/14/2018
54EYK12GINSENG (HERBAL & BOTANICAL TEAS)
2300DIETARYLBL
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
Division of Southeast Imports (DSEI)
5/2/2017
25LGT31GINSENG, DRIED OR PASTE (ROOT & TUBER VEGETABLE)
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/6/2017
31KYY99TEA, N.E.C.
256INCONSPICU
473LABELING
482NUTRIT LBL
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Daehan Red Ginseng Promotion Corporation's FDA import refusal history?

Daehan Red Ginseng Promotion Corporation (FEI: 3010187121) has 4 FDA import refusal record(s) in our database, spanning from 3/6/2017 to 2/8/2019.

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. Daehan Red Ginseng Promotion Corporation's FEI number is 3010187121.

What types of violations has Daehan Red Ginseng Promotion Corporation received?

Daehan Red Ginseng Promotion Corporation has been cited for 6 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 Daehan Red Ginseng Promotion Corporation come from?

All FDA import refusal data for Daehan Red Ginseng Promotion Corporation 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.