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Zegna-Daidong Ltd

⚠️ Moderate Risk

FEI: 3006473188 • Hong Kong • HONG KONG

FEI

FEI Number

3006473188

📍

Location

Hong Kong

🇭🇰

Country

HONG KONG
🏢

Address

Rooms 14-19 18/F Nan Fung Comm Centre19, , Hong Kong, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/12/2008
Latest Refusal
6/16/2008
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

472×

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
9/12/2008
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)
6/16/2008
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Zegna-Daidong Ltd's FDA import refusal history?

Zegna-Daidong Ltd (FEI: 3006473188) has 2 FDA import refusal record(s) in our database, spanning from 6/16/2008 to 9/12/2008.

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. Zegna-Daidong Ltd's FEI number is 3006473188.

What types of violations has Zegna-Daidong Ltd received?

Zegna-Daidong 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 Zegna-Daidong Ltd come from?

All FDA import refusal data for Zegna-Daidong 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.