Kenlex Technology Ltd
⚠️ Moderate Risk
FEI: 3005500076 • Huizhou, Guang Dong • CHINA
FEI Number
3005500076
Location
Huizhou, Guang Dong
Country
CHINAAddress
Block 2, Industry Basic; Sanxin Area, Huizhou, Guang Dong, 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
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
Refusal History
Frequently Asked Questions
What is Kenlex Technology Ltd's FDA import refusal history?
Kenlex Technology Ltd (FEI: 3005500076) has 3 FDA import refusal record(s) in our database, spanning from 8/22/2006 to 8/22/2006.
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. Kenlex Technology Ltd's FEI number is 3005500076.
What types of violations has Kenlex Technology Ltd received?
Kenlex Technology 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 Kenlex Technology Ltd come from?
All FDA import refusal data for Kenlex Technology 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.