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Sunfrom Pro Lighting Equipment Co., Limited

⚠️ Moderate Risk

FEI: 3009573602 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3009573602

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No. 2 Dalang, Baiyun, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/16/2012
Latest Refusal
8/16/2012
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
8/16/2012
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Sunfrom Pro Lighting Equipment Co., Limited's FDA import refusal history?

Sunfrom Pro Lighting Equipment Co., Limited (FEI: 3009573602) has 1 FDA import refusal record(s) in our database, spanning from 8/16/2012 to 8/16/2012.

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. Sunfrom Pro Lighting Equipment Co., Limited's FEI number is 3009573602.

What types of violations has Sunfrom Pro Lighting Equipment Co., Limited received?

Sunfrom Pro Lighting Equipment Co., Limited 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 Sunfrom Pro Lighting Equipment Co., Limited come from?

All FDA import refusal data for Sunfrom Pro Lighting Equipment Co., Limited 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.