Ground Tech Equipment Co., Ltd
⚠️ Moderate Risk
FEI: 3006768798 • Taiwan City Taiwan • TAIWAN
FEI Number
3006768798
Location
Taiwan City Taiwan
Country
TAIWANAddress
1f, No 18 Kai An 1th Street, , Taiwan City Taiwan, , Taiwan
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 PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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 |
|---|---|---|---|
| 10/8/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | Cincinnati District Office (CIN-DO) | |
| 1/30/2012 | 79OHJLOW ELECTRIC FIELD NON-THERMAL TISSUE ABLATION SYSTEM | 118NOT LISTED | San Francisco District Office (SAN-DO) |
| 7/25/2011 | 80KZFDEVICE, MEDICAL EXAMINATION, AC POWERED | 237NO PMA | San Francisco District Office (SAN-DO) |
| 10/19/2010 | 89KTBDEVICE, IONTOPHORESIS, SPECIFIC USES | 237NO PMA | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Ground Tech Equipment Co., Ltd's FDA import refusal history?
Ground Tech Equipment Co., Ltd (FEI: 3006768798) has 4 FDA import refusal record(s) in our database, spanning from 10/19/2010 to 10/8/2014.
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. Ground Tech Equipment Co., Ltd's FEI number is 3006768798.
What types of violations has Ground Tech Equipment Co., Ltd received?
Ground Tech Equipment 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 Ground Tech Equipment Co., Ltd come from?
All FDA import refusal data for Ground Tech Equipment 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.