HONG KONG BOROFONE TECHNOLOGY LT
⚠️ Moderate Risk
FEI: 3013208403 • HONG KONG • HONG KONG
FEI Number
3013208403
Location
HONG KONG
Country
HONG KONGAddress
RM D 10/F TOWER A BILLI, WANG KWONG RD KLN BAY HONG KONG, HONG KONG, , Hong Kong
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).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
Frequently Asked Questions
What is HONG KONG BOROFONE TECHNOLOGY LT's FDA import refusal history?
HONG KONG BOROFONE TECHNOLOGY LT (FEI: 3013208403) has 1 FDA import refusal record(s) in our database, spanning from 7/17/2018 to 7/17/2018.
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. HONG KONG BOROFONE TECHNOLOGY LT's FEI number is 3013208403.
What types of violations has HONG KONG BOROFONE TECHNOLOGY LT received?
HONG KONG BOROFONE TECHNOLOGY LT 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 HONG KONG BOROFONE TECHNOLOGY LT come from?
All FDA import refusal data for HONG KONG BOROFONE TECHNOLOGY LT 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.