Guangzhou Renlang Electronic Technology Co Ltd
⚠️ Moderate Risk
FEI: 3012252693 • Baiyun District Guangzhhou • CHINA
FEI Number
3012252693
Location
Baiyun District Guangzhhou
Country
CHINAAddress
Bldg F No 815, Congiun Rd Yuanxiagian, Baiyun District Guangzhhou, , 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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
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 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 Guangzhou Renlang Electronic Technology Co Ltd's FDA import refusal history?
Guangzhou Renlang Electronic Technology Co Ltd (FEI: 3012252693) has 1 FDA import refusal record(s) in our database, spanning from 5/11/2016 to 5/11/2016.
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. Guangzhou Renlang Electronic Technology Co Ltd's FEI number is 3012252693.
What types of violations has Guangzhou Renlang Electronic Technology Co Ltd received?
Guangzhou Renlang Electronic Technology Co Ltd has been cited for 4 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 Guangzhou Renlang Electronic Technology Co Ltd come from?
All FDA import refusal data for Guangzhou Renlang Electronic Technology Co Ltd 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.