Shenhou Guangming Ceramics Factory
⚠️ Moderate Risk
FEI: 3004481709 • 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
NO TAG
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/15/2015 | 95RDZLOW-POWER LASER LIGHT SHOW PROJECTOR, DISPLAY PRODUCTS | Seattle District Office (SEA-DO) | |
| 6/15/2015 | 95RDZLOW-POWER LASER LIGHT SHOW PROJECTOR, DISPLAY PRODUCTS | Seattle District Office (SEA-DO) | |
| 6/15/2015 | 95RDZLOW-POWER LASER LIGHT SHOW PROJECTOR, DISPLAY PRODUCTS | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Shenhou Guangming Ceramics Factory's FDA import refusal history?
Shenhou Guangming Ceramics Factory (FEI: 3004481709) has 3 FDA import refusal record(s) in our database, spanning from 6/15/2015 to 6/15/2015.
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. Shenhou Guangming Ceramics Factory's FEI number is 3004481709.
What types of violations has Shenhou Guangming Ceramics Factory received?
Shenhou Guangming Ceramics Factory 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 Shenhou Guangming Ceramics Factory come from?
All FDA import refusal data for Shenhou Guangming Ceramics Factory 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.