Lanson Optical Co., Ltd.
⚠️ Moderate Risk
FEI: 3004101655 • Wenzhou • CHINA
FEI Number
3004101655
Location
Wenzhou
Country
CHINAAddress
8F, Xincheng Bldg., Jinxiu Rd., , Wenzhou, , 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 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).
NOT IMPACT
The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/13/2013 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HOISPECTACLE, MAGNIFYING | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) | |
| 9/13/2013 | 86HQZFRAME, SPECTACLE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Lanson Optical Co., Ltd.'s FDA import refusal history?
Lanson Optical Co., Ltd. (FEI: 3004101655) has 15 FDA import refusal record(s) in our database, spanning from 9/13/2013 to 9/13/2013.
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. Lanson Optical Co., Ltd.'s FEI number is 3004101655.
What types of violations has Lanson Optical Co., Ltd. received?
Lanson Optical Co., Ltd. has been cited for 3 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 Lanson Optical Co., Ltd. come from?
All FDA import refusal data for Lanson Optical 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.