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Nel Ele

⚠️ Moderate Risk

FEI: 3003050510 • Kow • HONG KONG

FEI

FEI Number

3003050510

📍

Location

Kow

🇭🇰

Country

HONG KONG
🏢

Address

15, , Kow, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

39.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/12/2003
Latest Refusal
9/19/2002
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

474×

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
3/12/2003
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)
3/12/2003
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)
11/6/2002
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)
9/19/2002
95L32CD PLAYER COMBINATION SYSTEMS
47NON STD
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Nel Ele's FDA import refusal history?

Nel Ele (FEI: 3003050510) has 4 FDA import refusal record(s) in our database, spanning from 9/19/2002 to 3/12/2003.

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. Nel Ele's FEI number is 3003050510.

What types of violations has Nel Ele received?

Nel Ele 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 Nel Ele come from?

All FDA import refusal data for Nel Ele 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.