SHENZHEN QIANHAI KJONE TECHNOLOGY C
⚠️ Moderate Risk
FEI: 3017068033 • Guangzhou, Guangdong • CHINA
FEI Number
3017068033
Location
Guangzhou, Guangdong
Country
CHINAAddress
(Spb-A)(N3p) # 12, 309 West Of Tongda; Baiyun Sanxian Hebian St Baiyundis, Guangzhou, Guangdong, China
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).
NOT IMPACT
The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
Frequently Asked Questions
What is SHENZHEN QIANHAI KJONE TECHNOLOGY C's FDA import refusal history?
SHENZHEN QIANHAI KJONE TECHNOLOGY C (FEI: 3017068033) has 1 FDA import refusal record(s) in our database, spanning from 8/14/2020 to 8/14/2020.
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. SHENZHEN QIANHAI KJONE TECHNOLOGY C's FEI number is 3017068033.
What types of violations has SHENZHEN QIANHAI KJONE TECHNOLOGY C received?
SHENZHEN QIANHAI KJONE TECHNOLOGY C has been cited for 3 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 SHENZHEN QIANHAI KJONE TECHNOLOGY C come from?
All FDA import refusal data for SHENZHEN QIANHAI KJONE TECHNOLOGY C 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.