HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD
⚠️ Moderate Risk
FEI: 3011649813 • Shenzhen, Guangdong • CHINA
FEI Number
3011649813
Location
Shenzhen, Guangdong
Country
CHINAAddress
8F, Bldg 4,128# Shangnan East Rd, Bao'an, Shajing, Baoan, 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
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).
LBLG ADVER
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded because its labeling is misleading in a particular, namely that it fails to reveal facts (non-sterility) that are material with respect to consequences which may result from the use of the article according to the labeling, or advertising, or under such conditions of use as are customary or usual.
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/7/2021 | 83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM. | 508NO 510(K) | Division of Northern Border Imports (DNBI) |
| 7/6/2020 | 88NNKCONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE | Division of Southeast Imports (DSEI) | |
| 3/13/2019 | 88NNKCONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE | 2020LBLG ADVER | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD's FDA import refusal history?
HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD (FEI: 3011649813) has 3 FDA import refusal record(s) in our database, spanning from 3/13/2019 to 6/7/2021.
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. HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD's FEI number is 3011649813.
What types of violations has HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD received?
HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD has been cited for 5 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 HUACHENYANG(SHENZHEN)TECHNOLOGY CO., LTD come from?
All FDA import refusal data for HUACHENYANG(SHENZHEN)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.