ImportRefusal LogoImportRefusal

Shenzhen Master Optical Manufacturi

⚠️ Moderate Risk

FEI: 3008915208 • Shenzhenshenzhen • CHINA

FEI

FEI Number

3008915208

📍

Location

Shenzhenshenzhen

🇨🇳

Country

CHINA
🏢

Address

No. 44 Dafeng New Villagepa Kong Henggang, , Shenzhenshenzhen, , China

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
5/24/2011
Latest Refusal
5/24/2011
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
5/24/2011
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Seattle District Office (SEA-DO)
5/24/2011
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
118NOT LISTED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Shenzhen Master Optical Manufacturi's FDA import refusal history?

Shenzhen Master Optical Manufacturi (FEI: 3008915208) has 2 FDA import refusal record(s) in our database, spanning from 5/24/2011 to 5/24/2011.

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. Shenzhen Master Optical Manufacturi's FEI number is 3008915208.

What types of violations has Shenzhen Master Optical Manufacturi received?

Shenzhen Master Optical Manufacturi 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 Master Optical Manufacturi come from?

All FDA import refusal data for Shenzhen Master Optical Manufacturi 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.