SEESIL NTEUMM
⚠️ Moderate Risk
FEI: 3012848866 • SHENZHEN • CHINA
FEI Number
3012848866
Location
SHENZHEN
Country
CHINAAddress
4TH FLOOR 7TH BUILDING, , SHENZHEN, , 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 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 |
|---|---|---|---|
| 11/8/2016 | 95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL | 476NO REGISTR | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is SEESIL NTEUMM's FDA import refusal history?
SEESIL NTEUMM (FEI: 3012848866) has 1 FDA import refusal record(s) in our database, spanning from 11/8/2016 to 11/8/2016.
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. SEESIL NTEUMM's FEI number is 3012848866.
What types of violations has SEESIL NTEUMM received?
SEESIL NTEUMM 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 SEESIL NTEUMM come from?
All FDA import refusal data for SEESIL NTEUMM 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.