Shenzhen Dongdixin Technology Co Ltd
✅ Low Risk
FEI: 3011152125 • Zhenzhen • CHINA
FEI Number
3011152125
Location
Zhenzhen
Country
CHINAAddress
No 3 Bldg, Xilibaimang Xusheng Estate, , Zhenzhen, , China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/2/2017 | 89IPFSTIMULATOR, MUSCLE, POWERED | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 11/2/2017 | 89IPFSTIMULATOR, MUSCLE, POWERED | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 11/2/2017 | 68XYY99OTHER ANIMAL, N.E.C. DEVICE/DIAG PROD FOR ANIMAL | 118NOT LISTED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Shenzhen Dongdixin Technology Co Ltd's FDA import refusal history?
Shenzhen Dongdixin Technology Co Ltd (FEI: 3011152125) has 3 FDA import refusal record(s) in our database, spanning from 11/2/2017 to 11/2/2017.
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. Shenzhen Dongdixin Technology Co Ltd's FEI number is 3011152125.
What types of violations has Shenzhen Dongdixin Technology Co Ltd received?
Shenzhen Dongdixin 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 Dongdixin Technology Co Ltd come from?
All FDA import refusal data for Shenzhen Dongdixin 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.