Clement Li
⚠️ Moderate Risk
FEI: 3003609885 • Edmonton, AB • CANADA
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/30/2002 | 54AYY99VITAMIN, N.E.C. | 238UNSAFE ADD | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Clement Li's FDA import refusal history?
Clement Li (FEI: 3003609885) has 1 FDA import refusal record(s) in our database, spanning from 4/30/2002 to 4/30/2002.
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. Clement Li's FEI number is 3003609885.
What types of violations has Clement Li received?
Clement Li 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 Clement Li come from?
All FDA import refusal data for Clement Li 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.