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MIN JU KIM

⚠️ High Risk

FEI: 3040280652 • Sejong, Sejong • SOUTH KOREA

FEI

FEI Number

3040280652

📍

Location

Sejong, Sejong

🇰🇷
🏢

Address

Dongangu, Doum 5-Ro, Sejong, Sejong, South Korea

High Risk

FDA Import Risk Assessment

55.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
12/12/2025
Latest Refusal
10/29/2025
Earliest Refusal

Score Breakdown

Violation Severity
59.3×40%
Refusal Volume
25.9×30%
Recency
98.5×20%
Frequency
40.0×10%
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

1184×

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).

32804×

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.

5084×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

843×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
12/12/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Division of Southeast Imports (DSEI)
12/12/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Division of Southeast Imports (DSEI)
12/1/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Division of Southeast Imports (DSEI)
10/29/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is MIN JU KIM's FDA import refusal history?

MIN JU KIM (FEI: 3040280652) has 4 FDA import refusal record(s) in our database, spanning from 10/29/2025 to 12/12/2025.

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. MIN JU KIM's FEI number is 3040280652.

What types of violations has MIN JU KIM received?

MIN JU KIM has been cited for 4 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 MIN JU KIM come from?

All FDA import refusal data for MIN JU KIM 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.