ImportRefusal LogoImportRefusal

Danong

⚠️ Moderate Risk

FEI: 3004521899 • Gimpo • SOUTH KOREA

FEI

FEI Number

3004521899

📍

Location

Gimpo

🇰🇷
🏢

Address

4-20a 585-4 Wonsan-ri, , Gimpo, , South Korea

Moderate Risk

FDA Import Risk Assessment

49.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
1/21/2011
Latest Refusal
1/21/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

115×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
1/21/2011
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New York District Office (NYK-DO)
1/21/2011
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New York District Office (NYK-DO)
1/21/2011
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New York District Office (NYK-DO)
1/21/2011
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New York District Office (NYK-DO)
1/21/2011
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Danong's FDA import refusal history?

Danong (FEI: 3004521899) has 5 FDA import refusal record(s) in our database, spanning from 1/21/2011 to 1/21/2011.

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. Danong's FEI number is 3004521899.

What types of violations has Danong received?

Danong has been cited for 1 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 Danong come from?

All FDA import refusal data for Danong 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.