Quasar Engineering
⚠️ Moderate Risk
FEI: 3010042517 • Kowloon • CHINA
FEI Number
3010042517
Location
Kowloon
Country
CHINAAddress
495 Castle Peak Rd. Lai Chi Kok, , Kowloon, , 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/28/2018 | 74OADCATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FLUTTER | Division of Southeast Imports (DSEI) | |
| 9/28/2018 | 74OADCATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FLUTTER | Division of Southeast Imports (DSEI) | |
| 9/28/2018 | 74OADCATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FLUTTER | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Quasar Engineering's FDA import refusal history?
Quasar Engineering (FEI: 3010042517) has 3 FDA import refusal record(s) in our database, spanning from 9/28/2018 to 9/28/2018.
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. Quasar Engineering's FEI number is 3010042517.
What types of violations has Quasar Engineering received?
Quasar Engineering 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 Quasar Engineering come from?
All FDA import refusal data for Quasar Engineering 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.