Altix
⚠️ Moderate Risk
FEI: 3008939484 • Val de Reuil, Eure • FRANCE
FEI Number
3008939484
Location
Val de Reuil, Eure
Country
FRANCEAddress
4 Parc D Affaires des Portes, , Val de Reuil, Eure, 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
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/6/2013 | 95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS | 126FAILS STD | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Altix's FDA import refusal history?
Altix (FEI: 3008939484) has 1 FDA import refusal record(s) in our database, spanning from 8/6/2013 to 8/6/2013.
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. Altix's FEI number is 3008939484.
What types of violations has Altix received?
Altix 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 Altix come from?
All FDA import refusal data for Altix 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.