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Daedong Korea Ginseng Co., Ltd.

⚠️ High Risk

FEI: 3010102493 • Geumsan-gun, Chungcheongnam-do • SOUTH KOREA

FEI

FEI Number

3010102493

📍

Location

Geumsan-gun, Chungcheongnam-do

🇰🇷
🏢

Address

Gunbuk-myun, 586 Gunbuk-ro, Geumsan-gun, Chungcheongnam-do, South Korea

High Risk

FDA Import Risk Assessment

66.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

43
Total Refusals
20
Unique Violations
10/31/2025
Latest Refusal
9/18/2004
Earliest Refusal

Score Breakdown

Violation Severity
68.2×40%
Refusal Volume
60.9×30%
Recency
96.1×20%
Frequency
20.4×10%
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

292012×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

4828×

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.

487×

NEEDS ACID

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.

38987×

INADPRCCTL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate process controls.

1186×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

2604×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3064×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

2414×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

4722×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

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.

2561×

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)).

3201×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3211×

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.

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)).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

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.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
10/31/2025
20KYY04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES
3898INADPRCCTL
Division of Southeast Imports (DSEI)
5/9/2025
26CYT04OLIVE OIL, REFINED, SINGLE INGREDIENT
3898INADPRCCTL
Division of Southeast Imports (DSEI)
4/17/2024
28YGY99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
3898INADPRCCTL
48NEEDS ACID
Division of Northeast Imports (DNEI)
6/5/2023
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
3898INADPRCCTL
482NUTRIT LBL
Division of West Coast Imports (DWCI)
6/5/2023
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
3898INADPRCCTL
482NUTRIT LBL
Division of West Coast Imports (DWCI)
5/18/2023
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
3898INADPRCCTL
48NEEDS ACID
482NUTRIT LBL
Division of West Coast Imports (DWCI)
5/18/2023
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
3898INADPRCCTL
48NEEDS ACID
482NUTRIT LBL
Division of West Coast Imports (DWCI)
10/21/2022
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
48NEEDS ACID
482NUTRIT LBL
Division of West Coast Imports (DWCI)
10/21/2022
25MCT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
48NEEDS ACID
482NUTRIT LBL
Division of West Coast Imports (DWCI)
4/12/2021
25MVT31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/14/2020
25LYY31GINSENG, DRIED OR PASTE (ROOT & TUBER VEGETABLE)
48NEEDS ACID
Division of West Coast Imports (DWCI)
6/13/2018
25JGH31GINSENG (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of West Coast Imports (DWCI)
6/13/2018
25JGH31GINSENG (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of West Coast Imports (DWCI)
6/13/2018
25JGH31GINSENG (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of West Coast Imports (DWCI)
6/13/2018
25JGH31GINSENG (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of West Coast Imports (DWCI)
4/13/2018
25MCI31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
260FALSE
306INSANITARY
Division of West Coast Imports (DWCI)
4/13/2018
25MCI31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
260FALSE
306INSANITARY
Division of West Coast Imports (DWCI)
4/13/2018
25MCI31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
260FALSE
306INSANITARY
Division of West Coast Imports (DWCI)
4/13/2018
25MCI31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
260FALSE
306INSANITARY
Division of West Coast Imports (DWCI)
10/20/2017
54YBH04GINSENG UNCONVENTIONAL DIETARY SPECIALITY FOR HUMANS OR ANIMALS
2300DIETARYLBL
321LACKS N/C
473LABELING
Division of Southeast Imports (DSEI)
6/9/2017
25LGH31GINSENG, DRIED OR PASTE (ROOT & TUBER VEGETABLE)
48NEEDS ACID
Division of West Coast Imports (DWCI)
3/23/2017
54EBT12GINSENG (HERBAL & BOTANICAL TEAS)
320LACKS FIRM
324NO ENGLISH
488HEALTH C
Division of Southeast Imports (DSEI)
2/22/2017
54EBT12GINSENG (HERBAL & BOTANICAL TEAS)
256INCONSPICU
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
2/22/2017
66VIF99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
New Orleans District Office (NOL-DO)
11/9/2016
66VAB99MISCELLANEOUS PATENT MEDICINES, ETC.
472NO ENGLISH
Division of Southeast Imports (DSEI)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
10/10/2008
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
2920PESTICIDES
Los Angeles District Office (LOS-DO)
1/18/2006
54EBK12GINSENG (HERBAL & BOTANICAL TEAS)
472NO ENGLISH
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/18/2004
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Los Angeles District Office (LOS-DO)
9/18/2004
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Los Angeles District Office (LOS-DO)
9/18/2004
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
Los Angeles District Office (LOS-DO)
9/18/2004
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
Los Angeles District Office (LOS-DO)
9/18/2004
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Daedong Korea Ginseng Co., Ltd.'s FDA import refusal history?

Daedong Korea Ginseng Co., Ltd. (FEI: 3010102493) has 43 FDA import refusal record(s) in our database, spanning from 9/18/2004 to 10/31/2025.

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. Daedong Korea Ginseng Co., Ltd.'s FEI number is 3010102493.

What types of violations has Daedong Korea Ginseng Co., Ltd. received?

Daedong Korea Ginseng Co., Ltd. has been cited for 20 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 Daedong Korea Ginseng Co., Ltd. come from?

All FDA import refusal data for Daedong Korea Ginseng Co., 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.