KODAE COMMERCIAL COMPANY
⚠️ Moderate Risk
FEI: 3004394179 • Koyang, KYONGGi • SOUTH KOREA
FEI Number
3004394179
Location
Koyang, KYONGGi
Country
SOUTH KOREAAddress
Yongdudong 432 182, , Tokyang , Koyang, KYONGGi, 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
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/19/2004 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 5/19/2004 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 5/19/2004 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | 83NO PROCESS | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is KODAE COMMERCIAL COMPANY's FDA import refusal history?
KODAE COMMERCIAL COMPANY (FEI: 3004394179) has 3 FDA import refusal record(s) in our database, spanning from 5/19/2004 to 5/19/2004.
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. KODAE COMMERCIAL COMPANY's FEI number is 3004394179.
What types of violations has KODAE COMMERCIAL COMPANY received?
KODAE COMMERCIAL COMPANY 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 KODAE COMMERCIAL COMPANY come from?
All FDA import refusal data for KODAE COMMERCIAL COMPANY 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.