ImportRefusal LogoImportRefusal

Deokswung Mulsan Co.

⚠️ High Risk

FEI: 3003141235 • Kyeonggi • SOUTH KOREA

FEI

FEI Number

3003141235

📍

Location

Kyeonggi

🇰🇷
🏢

Address

262 Gamil Dong, , Kyeonggi, , South Korea

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/27/2003
Latest Refusal
4/1/2002
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
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

2494×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
3/27/2003
16AGH28POLLACK, POLLOCK
249FILTHY
Los Angeles District Office (LOS-DO)
3/27/2003
16MGH03SQUID, OTHER AQUATIC SPECIES
249FILTHY
Los Angeles District Office (LOS-DO)
4/1/2002
16AGH28POLLACK, POLLOCK
249FILTHY
Baltimore District Office (BLT-DO)
4/1/2002
16AGH28POLLACK, POLLOCK
249FILTHY
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Deokswung Mulsan Co.'s FDA import refusal history?

Deokswung Mulsan Co. (FEI: 3003141235) has 4 FDA import refusal record(s) in our database, spanning from 4/1/2002 to 3/27/2003.

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. Deokswung Mulsan Co.'s FEI number is 3003141235.

What types of violations has Deokswung Mulsan Co. received?

Deokswung Mulsan Co. 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 Deokswung Mulsan Co. come from?

All FDA import refusal data for Deokswung Mulsan Co. 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.