Ibeks Technologies Co., Ltd
⚠️ Moderate Risk
FEI: 3003467258 • Seoul • SOUTH KOREA
FEI Number
3003467258
Location
Seoul
Country
SOUTH KOREAAddress
6462 Naebalsan Dong Kangseo Ku, , 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is Ibeks Technologies Co., Ltd's FDA import refusal history?
Ibeks Technologies Co., Ltd (FEI: 3003467258) has 2 FDA import refusal record(s) in our database, spanning from 2/15/2002 to 2/15/2002.
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. Ibeks Technologies Co., Ltd's FEI number is 3003467258.
What types of violations has Ibeks Technologies Co., Ltd received?
Ibeks Technologies 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 Ibeks Technologies Co., Ltd come from?
All FDA import refusal data for Ibeks Technologies 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.