Guoteng Science Tech Deve Co Ltd
⚠️ Moderate Risk
FEI: 3007871360 • Zhuhaizhuhai • CHINA
FEI Number
3007871360
Location
Zhuhaizhuhai
Country
CHINAAddress
Three Dimension Science Techbldg No 184, , Zhuhaizhuhai, , 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.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/17/2013 | 74MWIMONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) | Cincinnati District Office (CIN-DO) | |
| 1/17/2013 | 74MWIMONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) | Cincinnati District Office (CIN-DO) | |
| 1/17/2013 | 74MWIMONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) | Cincinnati District Office (CIN-DO) | |
| 1/17/2013 | 74MWIMONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) | Cincinnati District Office (CIN-DO) | |
| 10/25/2012 | 74DRTMONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM) | Cincinnati District Office (CIN-DO) | |
| 7/19/2011 | 74MWIMONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Guoteng Science Tech Deve Co Ltd's FDA import refusal history?
Guoteng Science Tech Deve Co Ltd (FEI: 3007871360) has 6 FDA import refusal record(s) in our database, spanning from 7/19/2011 to 1/17/2013.
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. Guoteng Science Tech Deve Co Ltd's FEI number is 3007871360.
What types of violations has Guoteng Science Tech Deve Co Ltd received?
Guoteng Science Tech Deve Co Ltd has been cited for 4 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 Guoteng Science Tech Deve Co Ltd come from?
All FDA import refusal data for Guoteng Science Tech Deve 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.