GUANG ZHOU SHENG MEI ELECTRONIC
⚠️ Moderate Risk
FEI: 3013672135 • Guangzhou, Guangdong • CHINA
FEI Number
3013672135
Location
Guangzhou, Guangdong
Country
CHINAAddress
Long G 11, Beitai Road, 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).
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.
NON STD
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 offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
Refusal History
Frequently Asked Questions
What is GUANG ZHOU SHENG MEI ELECTRONIC's FDA import refusal history?
GUANG ZHOU SHENG MEI ELECTRONIC (FEI: 3013672135) has 1 FDA import refusal record(s) in our database, spanning from 8/17/2017 to 8/17/2017.
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. GUANG ZHOU SHENG MEI ELECTRONIC's FEI number is 3013672135.
What types of violations has GUANG ZHOU SHENG MEI ELECTRONIC received?
GUANG ZHOU SHENG MEI 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 GUANG ZHOU SHENG MEI ELECTRONIC come from?
All FDA import refusal data for GUANG ZHOU SHENG MEI 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.