Ningbo Ftz Yeayoo
⚠️ Moderate Risk
FEI: 3008254560 • Ningbo • 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
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/11/2012 | 53YK99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | 197COSM COLOR | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Ningbo Ftz Yeayoo's FDA import refusal history?
Ningbo Ftz Yeayoo (FEI: 3008254560) has 1 FDA import refusal record(s) in our database, spanning from 6/11/2012 to 6/11/2012.
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. Ningbo Ftz Yeayoo's FEI number is 3008254560.
What types of violations has Ningbo Ftz Yeayoo received?
Ningbo Ftz Yeayoo 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 Ningbo Ftz Yeayoo come from?
All FDA import refusal data for Ningbo Ftz Yeayoo 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.