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Kwangdong Pharmaceutical Co.,Ltd.

⚠️ High Risk

FEI: 3012290108 • Pyeongtaek, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3012290108

📍

Location

Pyeongtaek, Gyeonggi

🇰🇷
🏢

Address

1081 Gyeonggidae-Ro, , Pyeongtaek, Gyeonggi, South Korea

High Risk

FDA Import Risk Assessment

54.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
1/15/2026
Latest Refusal
3/21/2017
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
91.9×20%
Frequency
2.3×10%
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

38621×

DIETARYING

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)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.

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.

Refusal History

DateProductViolationsDivision
1/15/2026
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northeast Imports (DNEI)
3/21/2017
25MHE31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE)
3862DIETARYING
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Kwangdong Pharmaceutical Co.,Ltd.'s FDA import refusal history?

Kwangdong Pharmaceutical Co.,Ltd. (FEI: 3012290108) has 2 FDA import refusal record(s) in our database, spanning from 3/21/2017 to 1/15/2026.

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. Kwangdong Pharmaceutical Co.,Ltd.'s FEI number is 3012290108.

What types of violations has Kwangdong Pharmaceutical Co.,Ltd. received?

Kwangdong Pharmaceutical Co.,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 Kwangdong Pharmaceutical Co.,Ltd. come from?

All FDA import refusal data for Kwangdong Pharmaceutical 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.