ImportRefusal LogoImportRefusal

Shenzhen Quick Motion Development

⚠️ Moderate Risk

FEI: 3009860510 • Shenzhen • CHINA

FEI

FEI Number

3009860510

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Industrial Park #11 Zone 21, , Shenzhen, , 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
12/10/2012
Latest Refusal
12/10/2012
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
12/10/2012
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
476NO REGISTR
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Shenzhen Quick Motion Development's FDA import refusal history?

Shenzhen Quick Motion Development (FEI: 3009860510) has 1 FDA import refusal record(s) in our database, spanning from 12/10/2012 to 12/10/2012.

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. Shenzhen Quick Motion Development's FEI number is 3009860510.

What types of violations has Shenzhen Quick Motion Development received?

Shenzhen Quick Motion Development 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 Shenzhen Quick Motion Development come from?

All FDA import refusal data for Shenzhen Quick Motion Development 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.