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Andrea Pensbene

⚠️ Moderate Risk

FEI: 3003468758 • Palermo Partita • ITALY

FEI

FEI Number

3003468758

📍

Location

Palermo Partita

🇮🇹

Country

ITALY
🏢

Address

P.Zza Keibu N. 49, , Palermo Partita, , Italy

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
4/5/2007
Latest Refusal
4/5/2007
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

832×

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

DateProductViolationsDivision
4/5/2007
24UCE01ARTICHOKE, DRIED OR PASTE
83NO PROCESS
Baltimore District Office (BLT-DO)
4/5/2007
24UCE01ARTICHOKE, DRIED OR PASTE
83NO PROCESS
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Andrea Pensbene's FDA import refusal history?

Andrea Pensbene (FEI: 3003468758) has 2 FDA import refusal record(s) in our database, spanning from 4/5/2007 to 4/5/2007.

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. Andrea Pensbene's FEI number is 3003468758.

What types of violations has Andrea Pensbene received?

Andrea Pensbene 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 Andrea Pensbene come from?

All FDA import refusal data for Andrea Pensbene 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.