OKF Corporation
⚠️ Moderate Risk
FEI: 3010767692 • seoul • SOUTH KOREA
FEI Number
3010767692
Location
seoul
Country
SOUTH KOREAAddress
54 Hakdong ro 21-hil, Gangnam-gu, 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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
FALSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/3/2025 | 21DGC01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES | Division of Southeast Imports (DSEI) | |
| 2/3/2025 | 21DGC99MIXED FRUIT, JUICES OR CONCENTRATES N.E.C., | Division of Southeast Imports (DSEI) | |
| 6/26/2014 | 29AGI99NONCARBONATED SOFT DRINK, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is OKF Corporation's FDA import refusal history?
OKF Corporation (FEI: 3010767692) has 3 FDA import refusal record(s) in our database, spanning from 6/26/2014 to 2/3/2025.
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. OKF Corporation's FEI number is 3010767692.
What types of violations has OKF Corporation received?
OKF Corporation has been cited for 3 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 OKF Corporation come from?
All FDA import refusal data for OKF Corporation 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.