Shenzhen Sheng Yuan Heng Handicraft Co Ltd
⚠️ Moderate Risk
FEI: 3007201523 • Shen Zhen City • CHINA
FEI Number
3007201523
Location
Shen Zhen City
Country
CHINAAddress
123 You Ma Gang Industrict,Shi Wei Jian, , Shen Zhen City, , 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).
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.
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.
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.
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
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).
DV NAME
The article appears to be a device and its labeling fails to bear the proprietary or established name.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/22/2015 | 85HIHHYSTEROSCOPE (AND ACCESSORIES) | Seattle District Office (SEA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/4/2012 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Shenzhen Sheng Yuan Heng Handicraft Co Ltd's FDA import refusal history?
Shenzhen Sheng Yuan Heng Handicraft Co Ltd (FEI: 3007201523) has 11 FDA import refusal record(s) in our database, spanning from 1/4/2012 to 7/22/2015.
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 Sheng Yuan Heng Handicraft Co Ltd's FEI number is 3007201523.
What types of violations has Shenzhen Sheng Yuan Heng Handicraft Co Ltd received?
Shenzhen Sheng Yuan Heng Handicraft Co Ltd has been cited for 8 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 Sheng Yuan Heng Handicraft Co Ltd come from?
All FDA import refusal data for Shenzhen Sheng Yuan Heng Handicraft 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.