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Gemignani Tartufi

⚠️ Moderate Risk

FEI: 3010857980 • San Miniato, Pisa • ITALY

FEI

FEI Number

3010857980

📍

Location

San Miniato, Pisa

🇮🇹

Country

ITALY
🏢

Address

Viale Guglielmo Marconi 89, , San Miniato, Pisa, Italy

Moderate Risk

FDA Import Risk Assessment

43.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/3/2015
Latest Refusal
3/3/2015
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

624×

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).

Refusal History

DateProductViolationsDivision
3/3/2015
24CCN14STRINGBEAN, WITH SAUCE
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/3/2015
37JCN01BROWN SAUCE
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/3/2015
37JCN09WHITE SAUCE
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/3/2015
37JCN09WHITE SAUCE
62NEEDS FCE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Gemignani Tartufi's FDA import refusal history?

Gemignani Tartufi (FEI: 3010857980) has 4 FDA import refusal record(s) in our database, spanning from 3/3/2015 to 3/3/2015.

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. Gemignani Tartufi's FEI number is 3010857980.

What types of violations has Gemignani Tartufi received?

Gemignani Tartufi 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 Gemignani Tartufi come from?

All FDA import refusal data for Gemignani Tartufi 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.