SHENZHEN LIANFAXUN ELECTRONIC
⚠️ Moderate Risk
FEI: 3021724832 • Jiangxi • CHINA
FEI Number
3021724832
Location
Jiangxi
Country
CHINAAddress
No 59 Yinwang New Village, , Jiangxi, , 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
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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 SHENZHEN LIANFAXUN ELECTRONIC's FDA import refusal history?
SHENZHEN LIANFAXUN ELECTRONIC (FEI: 3021724832) has 1 FDA import refusal record(s) in our database, spanning from 3/21/2022 to 3/21/2022.
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 LIANFAXUN ELECTRONIC's FEI number is 3021724832.
What types of violations has SHENZHEN LIANFAXUN ELECTRONIC received?
SHENZHEN LIANFAXUN ELECTRONIC 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 SHENZHEN LIANFAXUN ELECTRONIC come from?
All FDA import refusal data for SHENZHEN LIANFAXUN ELECTRONIC 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.