Gelinova Srl
✅ Low Risk
FEI: 3002873553 • Pordenone, Pordenone • ITALY
FEI Number
3002873553
Location
Pordenone, Pordenone
Country
ITALYAddress
Via Pravolton 9/A, , Pordenone, Pordenone, 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
FLAVR LBLG
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an artificial flavoring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/19/2002 | 13GFT01ICE CREAM MIX | 258FLAVR LBLG | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Gelinova Srl's FDA import refusal history?
Gelinova Srl (FEI: 3002873553) has 1 FDA import refusal record(s) in our database, spanning from 3/19/2002 to 3/19/2002.
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. Gelinova Srl's FEI number is 3002873553.
What types of violations has Gelinova Srl received?
Gelinova 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 Gelinova Srl come from?
All FDA import refusal data for Gelinova 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.