Kinetec Sas Patterson Med
⚠️ Moderate Risk
FEI: 3009966647 • Charleville Mezieres • FRANCE
FEI Number
3009966647
Location
Charleville Mezieres
Country
FRANCEAddress
Zone Industrille De Mont 11 Ave, , Charleville Mezieres, , France
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
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
Frequently Asked Questions
What is Kinetec Sas Patterson Med's FDA import refusal history?
Kinetec Sas Patterson Med (FEI: 3009966647) has 3 FDA import refusal record(s) in our database, spanning from 3/14/2014 to 3/14/2014.
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. Kinetec Sas Patterson Med's FEI number is 3009966647.
What types of violations has Kinetec Sas Patterson Med received?
Kinetec Sas Patterson Med has been cited for 1 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 Kinetec Sas Patterson Med come from?
All FDA import refusal data for Kinetec Sas Patterson Med 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.