Beijing Sundor Laser Equipment Co. Ltd.
⚠️ Moderate Risk
FEI: 3014741352 • Beijing, Beijing • CHINA
FEI Number
3014741352
Location
Beijing, Beijing
Country
CHINAAddress
#3 FLOOR, BUILDING 16, JINGSHENG SOUTH 4TH STREET., JINQIAO S&T INDUSTRIAL BASE. ZHONGGUANCUN, Beijing, Beijing, 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
NON STD
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 offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
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 |
|---|---|---|---|
| 10/4/2023 | 95RHKLASER MARKER OR ENGRAVER | Division of West Coast Imports (DWCI) | |
| 3/10/2021 | 95RHKLASER MARKER OR ENGRAVER | Division of West Coast Imports (DWCI) | |
| 9/28/2020 | 95RHKLASER MARKER OR ENGRAVER | 47NON STD | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Beijing Sundor Laser Equipment Co. Ltd.'s FDA import refusal history?
Beijing Sundor Laser Equipment Co. Ltd. (FEI: 3014741352) has 3 FDA import refusal record(s) in our database, spanning from 9/28/2020 to 10/4/2023.
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. Beijing Sundor Laser Equipment Co. Ltd.'s FEI number is 3014741352.
What types of violations has Beijing Sundor Laser Equipment Co. Ltd. received?
Beijing Sundor Laser Equipment Co. Ltd. has been cited for 3 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 Beijing Sundor Laser Equipment Co. Ltd. come from?
All FDA import refusal data for Beijing Sundor Laser Equipment 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.