Alitrans Srl
✅ Low Risk
FEI: 3002912420 • Verona, Verona • ITALY
FEI Number
3002912420
Location
Verona, Verona
Country
ITALYAddress
Via Sei Maggio S1, , Verona, Verona, Italy
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/15/2005 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 198COLOR LBLG | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Alitrans Srl's FDA import refusal history?
Alitrans Srl (FEI: 3002912420) has 1 FDA import refusal record(s) in our database, spanning from 9/15/2005 to 9/15/2005.
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. Alitrans Srl's FEI number is 3002912420.
What types of violations has Alitrans Srl received?
Alitrans Srl 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 Alitrans Srl come from?
All FDA import refusal data for Alitrans Srl 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.