Intop Tech Co Ltd 2005 Dragon Bearl
⚠️ Moderate Risk
FEI: 3006528349 • Shanghai, Shanghai • CHINA
FEI Number
3006528349
Location
Shanghai, Shanghai
Country
CHINAAddress
Zhonghuanguangchang No, 2123 Pudonga Ve, Shanghai, Shanghai, 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
DE IMP GMP
The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).
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.
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/8/2013 | 89LYGMASSAGER, THERAPEUTIC, MANUAL | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 89LYGMASSAGER, THERAPEUTIC, MANUAL | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | 290DE IMP GMP | Seattle District Office (SEA-DO) |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | 290DE IMP GMP | Seattle District Office (SEA-DO) |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 89LYGMASSAGER, THERAPEUTIC, MANUAL | Seattle District Office (SEA-DO) | |
| 8/9/2013 | 87HSTAPPARATUS, TRACTION, NON-POWERED | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Intop Tech Co Ltd 2005 Dragon Bearl's FDA import refusal history?
Intop Tech Co Ltd 2005 Dragon Bearl (FEI: 3006528349) has 9 FDA import refusal record(s) in our database, spanning from 8/9/2013 to 11/8/2013.
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. Intop Tech Co Ltd 2005 Dragon Bearl's FEI number is 3006528349.
What types of violations has Intop Tech Co Ltd 2005 Dragon Bearl received?
Intop Tech Co Ltd 2005 Dragon Bearl 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 Intop Tech Co Ltd 2005 Dragon Bearl come from?
All FDA import refusal data for Intop Tech Co Ltd 2005 Dragon Bearl 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.