JEIL MEDICAL CORPO
⚠️ Moderate Risk
FEI: 3014282577 • Seoul • SOUTH KOREA
FEI Number
3014282577
Location
Seoul
Country
SOUTH KOREAAddress
#707, Kolon Scienc, , Seoul, , South Korea
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
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 |
|---|---|---|---|
| 5/18/2023 | 76JEYPLATE, BONE | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is JEIL MEDICAL CORPO's FDA import refusal history?
JEIL MEDICAL CORPO (FEI: 3014282577) has 1 FDA import refusal record(s) in our database, spanning from 5/18/2023 to 5/18/2023.
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. JEIL MEDICAL CORPO's FEI number is 3014282577.
What types of violations has JEIL MEDICAL CORPO received?
JEIL MEDICAL CORPO 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 JEIL MEDICAL CORPO come from?
All FDA import refusal data for JEIL MEDICAL CORPO 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.