Luxitalia Srl
⚠️ Moderate Risk
FEI: 3005204538 • San Pietro Vernotico, Brindisi • ITALY
FEI Number
3005204538
Location
San Pietro Vernotico, Brindisi
Country
ITALYAddress
Via Mare 92/94, , San Pietro Vernotico, Brindisi, Italy
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
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/26/2007 | 24HCO07PEPPER, SWEET, DRIED OR PASTE | Los Angeles District Office (LOS-DO) | |
| 7/26/2007 | 24HCO07PEPPER, SWEET, DRIED OR PASTE | Los Angeles District Office (LOS-DO) | |
| 7/26/2007 | 24ACO09MUNG BEAN | Los Angeles District Office (LOS-DO) | |
| 7/26/2007 | 24ACO09MUNG BEAN | Los Angeles District Office (LOS-DO) | |
| 7/26/2007 | 24TCO01ARTICHOKE (LEAF & STEM VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 7/26/2007 | 24TCO01ARTICHOKE (LEAF & STEM VEGETABLE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Luxitalia Srl's FDA import refusal history?
Luxitalia Srl (FEI: 3005204538) has 6 FDA import refusal record(s) in our database, spanning from 7/26/2007 to 7/26/2007.
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. Luxitalia Srl's FEI number is 3005204538.
What types of violations has Luxitalia Srl received?
Luxitalia Srl has been cited for 5 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 Luxitalia Srl come from?
All FDA import refusal data for Luxitalia 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.