Khidi
⚠️ Moderate Risk
FEI: 3005894081 • Dongkal-Gu Seoul Korea • SOUTH KOREA
FEI Number
3005894081
Location
Dongkal-Gu Seoul Korea
Country
SOUTH KOREAAddress
57-1 Noryang Jin-Dong, , Dongkal-Gu Seoul Korea, , 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
Frequently Asked Questions
What is Khidi's FDA import refusal history?
Khidi (FEI: 3005894081) has 2 FDA import refusal record(s) in our database, spanning from 10/17/2006 to 10/17/2006.
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. Khidi's FEI number is 3005894081.
What types of violations has Khidi received?
Khidi 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 Khidi come from?
All FDA import refusal data for Khidi 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.