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Guangzhou Yilong Technology Co Ltd

⚠️ Moderate Risk

FEI: 3009093143 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3009093143

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Tianhe 900, Beilu; Nanling Gongye, 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
10/10/2011
Latest Refusal
10/10/2011
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
10/10/2011
95RFELASER CUTTER, MATERIAL PROCESSING LASER PRODUCTS
476NO REGISTR
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Guangzhou Yilong Technology Co Ltd's FDA import refusal history?

Guangzhou Yilong Technology Co Ltd (FEI: 3009093143) has 1 FDA import refusal record(s) in our database, spanning from 10/10/2011 to 10/10/2011.

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. Guangzhou Yilong Technology Co Ltd's FEI number is 3009093143.

What types of violations has Guangzhou Yilong Technology Co Ltd received?

Guangzhou Yilong Technology Co 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 Guangzhou Yilong Technology Co Ltd come from?

All FDA import refusal data for Guangzhou Yilong Technology Co 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.