Cenexi
⚠️ Moderate Risk
FEI: 3007250542 • Fontenay-Sous-Bois, Val-de-Marne • FRANCE
FEI Number
3007250542
Location
Fontenay-Sous-Bois, Val-de-Marne
Country
FRANCEAddress
52 Rue Marcel Et Jacques Gaucher, , Fontenay-Sous-Bois, Val-de-Marne, 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/7/2020 | 63NCH25URSODIOL (CHOLINERGIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 9/26/2018 | 66KCA99THYROID INHIBITOR N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/15/2018 | 63BCP22TERBUTALINE SULFATE (BRONCHODILATOR) | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 10/21/2016 | 61GDL57SULFAMETHOXAZOLE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 10/21/2016 | 61GDL57SULFAMETHOXAZOLE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 10/12/2012 | 63BDK22TERBUTALINE SULFATE (BRONCHODILATOR) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 4/8/2009 | 60QCK82FLUMAZENIL (ANESTHETIC) | 75UNAPPROVED | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Cenexi's FDA import refusal history?
Cenexi (FEI: 3007250542) has 7 FDA import refusal record(s) in our database, spanning from 4/8/2009 to 1/7/2020.
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. Cenexi's FEI number is 3007250542.
What types of violations has Cenexi received?
Cenexi has been cited for 2 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 Cenexi come from?
All FDA import refusal data for Cenexi 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.