Mentor Optical Limited
⚠️ Moderate Risk
FEI: 3010256506 • Dong Guan, Guangdong • CHINA
FEI Number
3010256506
Location
Dong Guan, Guangdong
Country
CHINAAddress
Yuxian Road No 6, Baoshan Industrial, Zone Zhangmutouzhen, Dong Guan, Guangdong, 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 |
|---|---|---|---|
| 4/21/2016 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | 235NOT IMPACT | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Mentor Optical Limited's FDA import refusal history?
Mentor Optical Limited (FEI: 3010256506) has 1 FDA import refusal record(s) in our database, spanning from 4/21/2016 to 4/21/2016.
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. Mentor Optical Limited's FEI number is 3010256506.
What types of violations has Mentor Optical Limited received?
Mentor Optical 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 Mentor Optical Limited come from?
All FDA import refusal data for Mentor Optical 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.