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Guang Feng Enterprises Ltd.

⚠️ Moderate Risk

FEI: 3004618909 • Hong Kong • HONG KONG

FEI

FEI Number

3004618909

📍

Location

Hong Kong

🇭🇰

Country

HONG KONG
🏢

Address

130-136 Connaught Road, , Hong Kong, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

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

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

471×

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
95L22LASER PRODUCT FOR NON-MEDICAL USE
47NON STD
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Guang Feng Enterprises Ltd.'s FDA import refusal history?

Guang Feng Enterprises Ltd. (FEI: 3004618909) has 1 FDA import refusal record(s) in our database, spanning from 10/6/2005 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. Guang Feng Enterprises Ltd.'s FEI number is 3004618909.

What types of violations has Guang Feng Enterprises Ltd. received?

Guang Feng Enterprises 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 Guang Feng Enterprises Ltd. come from?

All FDA import refusal data for Guang Feng Enterprises 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.