Lelejia Medical Te
✅ Low Risk
FEI: 3006169336 • Beijing • CHINA
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/24/2008 | 76ELLTEETH, PORCELAIN | 341REGISTERED | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Lelejia Medical Te's FDA import refusal history?
Lelejia Medical Te (FEI: 3006169336) has 1 FDA import refusal record(s) in our database, spanning from 10/24/2008 to 10/24/2008.
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. Lelejia Medical Te's FEI number is 3006169336.
What types of violations has Lelejia Medical Te received?
Lelejia Medical Te 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 Lelejia Medical Te come from?
All FDA import refusal data for Lelejia Medical Te 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.