K & D (Macau) Development Ltd
⚠️ Moderate Risk
FEI: 3007544581 • Juk Mun • MACAU
FEI Number
3007544581
Location
Juk Mun
Country
MACAUAddress
Sung Juk Saang Gwong Coeng, Heng Long, Juk Mun, , Macau
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 K & D (Macau) Development Ltd's FDA import refusal history?
K & D (Macau) Development Ltd (FEI: 3007544581) has 2 FDA import refusal record(s) in our database, spanning from 8/17/2009 to 8/17/2009.
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. K & D (Macau) Development Ltd's FEI number is 3007544581.
What types of violations has K & D (Macau) Development Ltd received?
K & D (Macau) Development 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 K & D (Macau) Development Ltd come from?
All FDA import refusal data for K & D (Macau) Development 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.