Lee Chao Chang
⚠️ Moderate Risk
FEI: 3004528598 • Taoyuan • TAIWAN
FEI Number
3004528598
Location
Taoyuan
Country
TAIWANAddress
354 Chieh Shou Road, , Taoyuan, , Taiwan
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
STD LABEL
The article appears to not bear labeling prescribed by the performance standard established under section 514.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is Lee Chao Chang's FDA import refusal history?
Lee Chao Chang (FEI: 3004528598) has 1 FDA import refusal record(s) in our database, spanning from 3/3/2005 to 3/3/2005.
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. Lee Chao Chang's FEI number is 3004528598.
What types of violations has Lee Chao Chang received?
Lee Chao Chang 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 Lee Chao Chang come from?
All FDA import refusal data for Lee Chao Chang 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.