Shenzhen Nuozhe Technology Co Ltd
⚠️ Moderate Risk
FEI: 3011990627 • Shenzhen • CHINA
FEI Number
3011990627
Location
Shenzhen
Country
CHINAAddress
501.502 East, 5 Floor 2 Bldg, No. 28, , Shenzhen, , China
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
NOT IMPACT
The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/27/2017 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | 235NOT IMPACT | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Shenzhen Nuozhe Technology Co Ltd's FDA import refusal history?
Shenzhen Nuozhe Technology Co Ltd (FEI: 3011990627) has 1 FDA import refusal record(s) in our database, spanning from 3/27/2017 to 3/27/2017.
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 Nuozhe Technology Co Ltd's FEI number is 3011990627.
What types of violations has Shenzhen Nuozhe Technology Co Ltd received?
Shenzhen Nuozhe 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 Shenzhen Nuozhe Technology Co Ltd come from?
All FDA import refusal data for Shenzhen Nuozhe 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.