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Guangzhou Baiyun Shijing Minglia

⚠️ Moderate Risk

FEI: 3010338869 • Daiyun • CHINA

FEI

FEI Number

3010338869

📍

Location

Daiyun

🇨🇳

Country

CHINA
🏢

Address

C2 Building 11 Industry, , Daiyun, , 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
9/16/2013
Latest Refusal
9/16/2013
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
9/16/2013
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Guangzhou Baiyun Shijing Minglia's FDA import refusal history?

Guangzhou Baiyun Shijing Minglia (FEI: 3010338869) has 1 FDA import refusal record(s) in our database, spanning from 9/16/2013 to 9/16/2013.

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 Baiyun Shijing Minglia's FEI number is 3010338869.

What types of violations has Guangzhou Baiyun Shijing Minglia received?

Guangzhou Baiyun Shijing Minglia 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 Baiyun Shijing Minglia come from?

All FDA import refusal data for Guangzhou Baiyun Shijing Minglia 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.