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AOKER EYEWEAR MANUFACTORY LIMITED

⚠️ Moderate Risk

FEI: 3013688041 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3013688041

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Xiandong,SiLian Industrial, HengGang, LongGang, , Shenzhen, 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
9/13/2019
Latest Refusal
9/13/2019
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

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

Refusal History

DateProductViolationsDivision
9/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AOKER EYEWEAR MANUFACTORY LIMITED's FDA import refusal history?

AOKER EYEWEAR MANUFACTORY LIMITED (FEI: 3013688041) has 1 FDA import refusal record(s) in our database, spanning from 9/13/2019 to 9/13/2019.

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. AOKER EYEWEAR MANUFACTORY LIMITED's FEI number is 3013688041.

What types of violations has AOKER EYEWEAR MANUFACTORY LIMITED received?

AOKER EYEWEAR MANUFACTORY 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 AOKER EYEWEAR MANUFACTORY LIMITED come from?

All FDA import refusal data for AOKER EYEWEAR MANUFACTORY 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.