Chiun Shiu Enterprise Co Ltd
✅ Low Risk
FEI: 3004080297 • Miaoli • TAIWAN
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
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/6/2006 | 53LY99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Chiun Shiu Enterprise Co Ltd's FDA import refusal history?
Chiun Shiu Enterprise Co Ltd (FEI: 3004080297) has 1 FDA import refusal record(s) in our database, spanning from 3/6/2006 to 3/6/2006.
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. Chiun Shiu Enterprise Co Ltd's FEI number is 3004080297.
What types of violations has Chiun Shiu Enterprise Co Ltd received?
Chiun Shiu Enterprise Co 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 Chiun Shiu Enterprise Co Ltd come from?
All FDA import refusal data for Chiun Shiu Enterprise 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.