Guangzhou Xianda Spectacles Manufacture Co. Ltd.
⚠️ Moderate Risk
FEI: 3003583637 • Guangzhou, Guangdong • CHINA
FEI Number
3003583637
Location
Guangzhou, Guangdong
Country
CHINAAddress
Town, Peng Shang Xin Laneroad, Guangzhou, 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
LENS CERT
The lenses are declared by accompanying certificate to meet the requirements for impact-resistant lenses in 21 CFR 801.410 but does not appear to be impact-resistant.
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
Frequently Asked Questions
What is Guangzhou Xianda Spectacles Manufacture Co. Ltd.'s FDA import refusal history?
Guangzhou Xianda Spectacles Manufacture Co. Ltd. (FEI: 3003583637) has 2 FDA import refusal record(s) in our database, spanning from 11/25/2011 to 5/26/2015.
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. Guangzhou Xianda Spectacles Manufacture Co. Ltd.'s FEI number is 3003583637.
What types of violations has Guangzhou Xianda Spectacles Manufacture Co. Ltd. received?
Guangzhou Xianda Spectacles Manufacture Co. Ltd. has been cited for 2 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 Guangzhou Xianda Spectacles Manufacture Co. Ltd. come from?
All FDA import refusal data for Guangzhou Xianda Spectacles Manufacture 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.