YJK TECHNOLOGY(SHENZHEN) CO.,LIM
⚠️ Moderate Risk
FEI: 3015420315 • Shenzhen • CHINA
FEI Number
3015420315
Location
Shenzhen
Country
CHINAAddress
Building Floor5, 1 West,D, Shenzhen, , 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).
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
NO TAG
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).
STD LABEL
The article appears to not bear labeling prescribed by the performance standard established under section 514.
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.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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 YJK TECHNOLOGY(SHENZHEN) CO.,LIM's FDA import refusal history?
YJK TECHNOLOGY(SHENZHEN) CO.,LIM (FEI: 3015420315) has 2 FDA import refusal record(s) in our database, spanning from 12/18/2024 to 1/8/2025.
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. YJK TECHNOLOGY(SHENZHEN) CO.,LIM's FEI number is 3015420315.
What types of violations has YJK TECHNOLOGY(SHENZHEN) CO.,LIM received?
YJK TECHNOLOGY(SHENZHEN) CO.,LIM has been cited for 7 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 YJK TECHNOLOGY(SHENZHEN) CO.,LIM come from?
All FDA import refusal data for YJK TECHNOLOGY(SHENZHEN) CO.,LIM 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.