SHENZHEN HUI CHENG ELECTRONIC
⚠️ Moderate Risk
FEI: 3015092024 • Shenzhen • CHINA
FEI Number
3015092024
Location
Shenzhen
Country
CHINAAddress
South China City Exchange, Square 1 4 Floor, 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).
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.
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
Frequently Asked Questions
What is SHENZHEN HUI CHENG ELECTRONIC's FDA import refusal history?
SHENZHEN HUI CHENG ELECTRONIC (FEI: 3015092024) has 1 FDA import refusal record(s) in our database, spanning from 8/27/2019 to 8/27/2019.
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 HUI CHENG ELECTRONIC's FEI number is 3015092024.
What types of violations has SHENZHEN HUI CHENG ELECTRONIC received?
SHENZHEN HUI CHENG ELECTRONIC 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 HUI CHENG ELECTRONIC come from?
All FDA import refusal data for SHENZHEN HUI CHENG 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.