Tongyeong Melchi
⚠️ Moderate Risk
FEI: 3009094092 • Kyongnam • SOUTH KOREA
FEI Number
3009094092
Location
Kyongnam
Country
SOUTH KOREAAddress
177-181, Seohodon Tongyeong City, , Kyongnam, , 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
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
Frequently Asked Questions
What is Tongyeong Melchi's FDA import refusal history?
Tongyeong Melchi (FEI: 3009094092) has 2 FDA import refusal record(s) in our database, spanning from 4/15/2014 to 4/15/2014.
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. Tongyeong Melchi's FEI number is 3009094092.
What types of violations has Tongyeong Melchi received?
Tongyeong Melchi 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 Tongyeong Melchi come from?
All FDA import refusal data for Tongyeong Melchi 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.