Hyun Dae Pharmacy Co Ltd
✅ Low Risk
FEI: 3002468937 • Seoul • SOUTH KOREA
FEI Number
3002468937
Location
Seoul
Country
SOUTH KOREAAddress
213 Sosabon Donb, , Seoul, , 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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/16/2004 | 29ACT99NONCARBONATED SOFT DRINK, N.E.C. | 473LABELING | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Hyun Dae Pharmacy Co Ltd's FDA import refusal history?
Hyun Dae Pharmacy Co Ltd (FEI: 3002468937) has 1 FDA import refusal record(s) in our database, spanning from 12/16/2004 to 12/16/2004.
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. Hyun Dae Pharmacy Co Ltd's FEI number is 3002468937.
What types of violations has Hyun Dae Pharmacy Co Ltd received?
Hyun Dae Pharmacy Co Ltd 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 Hyun Dae Pharmacy Co Ltd come from?
All FDA import refusal data for Hyun Dae Pharmacy 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.