SHINRIM MULSAN
⚠️ High Risk
FEI: 3006396804 • Seoul, KR-11 • SOUTH KOREA
FEI Number
3006396804
Location
Seoul, KR-11
Country
SOUTH KOREAAddress
501, 166-8, Sukchon, Songpa, , Seoul, KR-11, South Korea
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AFN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AFN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AFN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 8/8/2012 | 16AGN01ANCHOVY | 308MFR INSAN | Division of Northeast Imports (DNEI) |
| 6/13/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 6/13/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 6/1/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 6/1/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 6/1/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 6/1/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/4/2012 | 16AFT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/3/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 4/3/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 4/3/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 4/3/2012 | 16AFH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 4/3/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
| 4/3/2012 | 16AGH01ANCHOVY | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is SHINRIM MULSAN's FDA import refusal history?
SHINRIM MULSAN (FEI: 3006396804) has 31 FDA import refusal record(s) in our database, spanning from 4/3/2012 to 8/8/2012.
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. SHINRIM MULSAN's FEI number is 3006396804.
What types of violations has SHINRIM MULSAN received?
SHINRIM MULSAN 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 SHINRIM MULSAN come from?
All FDA import refusal data for SHINRIM MULSAN 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.