KEYMOND GROUP
✅ Low Risk
FEI: 3013691891 • Kwun Tong, Kowloon • HONG KONG
FEI Number
3013691891
Location
Kwun Tong, Kowloon
Country
HONG KONGAddress
Unit A, 167 F, G; 169 Hoi Bun Road; Town, Kwun Tong, Kowloon, Hong Kong
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
Frequently Asked Questions
What is KEYMOND GROUP's FDA import refusal history?
KEYMOND GROUP (FEI: 3013691891) has 1 FDA import refusal record(s) in our database, spanning from 9/1/2017 to 9/1/2017.
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. KEYMOND GROUP's FEI number is 3013691891.
What types of violations has KEYMOND GROUP received?
KEYMOND GROUP has been cited for 2 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 KEYMOND GROUP come from?
All FDA import refusal data for KEYMOND GROUP 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.