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Denco Int'L Ltd

⚠️ Moderate Risk

FEI: 3003353423 • Kowloon • HONG KONG

FEI

FEI Number

3003353423

📍

Location

Kowloon

🇭🇰

Country

HONG KONG
🏢

Address

Unit 15-17, 9/F Chevalier Comm.Ctr, , Kowloon Bay, Kowloon, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/6/2005
Latest Refusal
9/7/2005
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

473×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

Refusal History

DateProductViolationsDivision
10/6/2005
95L31CD PLAYERS (COMPACT DISC PLAYERS)
47NON STD
Division of Southeast Imports (DSEI)
10/6/2005
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Division of Southeast Imports (DSEI)
9/7/2005
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Denco Int'L Ltd's FDA import refusal history?

Denco Int'L Ltd (FEI: 3003353423) has 3 FDA import refusal record(s) in our database, spanning from 9/7/2005 to 10/6/2005.

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. Denco Int'L Ltd's FEI number is 3003353423.

What types of violations has Denco Int'L Ltd received?

Denco Int'L Ltd 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 Denco Int'L Ltd come from?

All FDA import refusal data for Denco Int'L 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.