Shenzhen Huawen Technology Co.,Ltd
⚠️ Moderate Risk
FEI: 3014837396 • Shenzhen, Guangdong • CHINA
FEI Number
3014837396
Location
Shenzhen, Guangdong
Country
CHINAAddress
301 Building 4, Guorun Industrial Area, Zhonghua Road, Minzhi Street, Longhua District, , Shenzhen, 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
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.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/10/2020 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | Division of Southeast Imports (DSEI) | |
| 9/30/2020 | 80PXHTHERMOMETER KIT | 3280FRNMFGREG | Division of Southwest Imports (DSWI) |
| 9/18/2020 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | Division of Southeast Imports (DSEI) | |
| 7/24/2020 | 80LRJDISINFECTANT, MEDICAL DEVICES | Division of West Coast Imports (DWCI) | |
| 6/29/2020 | 80LRJDISINFECTANT, MEDICAL DEVICES | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Shenzhen Huawen Technology Co.,Ltd's FDA import refusal history?
Shenzhen Huawen Technology Co.,Ltd (FEI: 3014837396) has 5 FDA import refusal record(s) in our database, spanning from 6/29/2020 to 12/10/2020.
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 Huawen Technology Co.,Ltd's FEI number is 3014837396.
What types of violations has Shenzhen Huawen Technology Co.,Ltd received?
Shenzhen Huawen Technology Co.,Ltd 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 Huawen Technology Co.,Ltd come from?
All FDA import refusal data for Shenzhen Huawen 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.