ALPINION MEDICAL SYSTEMS
✅ Low Risk
FEI: 3014623413 • Anyang • SOUTH KOREA
FEI Number
3014623413
Location
Anyang
Country
SOUTH KOREAAddress
77 Heungan-Daero 81beon, , Anyang, , South Korea
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2019 | 90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is ALPINION MEDICAL SYSTEMS's FDA import refusal history?
ALPINION MEDICAL SYSTEMS (FEI: 3014623413) has 1 FDA import refusal record(s) in our database, spanning from 11/22/2019 to 11/22/2019.
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. ALPINION MEDICAL SYSTEMS's FEI number is 3014623413.
What types of violations has ALPINION MEDICAL SYSTEMS received?
ALPINION MEDICAL SYSTEMS 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 ALPINION MEDICAL SYSTEMS come from?
All FDA import refusal data for ALPINION MEDICAL SYSTEMS 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.