SHENZHEN QIANJIANG TECHNOLOGY CO., LTD
⚠️ High Risk
FEI: 3025358970 • Shenzhen, Guangdong • CHINA
FEI Number
3025358970
Location
Shenzhen, Guangdong
Country
CHINAAddress
401 No. 2, Tongqing Road, Tongxin Community, Baolong Street, Longgang District, , Shenzhen, Guangdong, China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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.
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/18/2026 | 79GFEBRUSH, DERMABRASION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 7/3/2025 | 79GFEBRUSH, DERMABRASION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 12/10/2024 | 79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SHENZHEN QIANJIANG TECHNOLOGY CO., LTD's FDA import refusal history?
SHENZHEN QIANJIANG TECHNOLOGY CO., LTD (FEI: 3025358970) has 3 FDA import refusal record(s) in our database, spanning from 12/10/2024 to 1/18/2026.
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 QIANJIANG TECHNOLOGY CO., LTD's FEI number is 3025358970.
What types of violations has SHENZHEN QIANJIANG TECHNOLOGY CO., LTD received?
SHENZHEN QIANJIANG TECHNOLOGY CO., LTD has been cited for 2 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 QIANJIANG TECHNOLOGY CO., LTD come from?
All FDA import refusal data for SHENZHEN QIANJIANG 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.