ImportRefusal LogoImportRefusal

Goccia Umbra S.N.C.

⚠️ Moderate Risk

FEI: 1000409065 • Castel Viscardo, TR • ITALY

FEI

FEI Number

1000409065

📍

Location

Castel Viscardo, TR

🇮🇹

Country

ITALY
🏢

Address

Podere Vitiano, , Castel Viscardo, TR, Italy

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
8/10/2004
Latest Refusal
8/10/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

625×

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
8/10/2004
37KGT99PASTES, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)
8/10/2004
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)
8/10/2004
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)
8/10/2004
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)
8/10/2004
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)

Frequently Asked Questions

What is Goccia Umbra S.N.C.'s FDA import refusal history?

Goccia Umbra S.N.C. (FEI: 1000409065) has 5 FDA import refusal record(s) in our database, spanning from 8/10/2004 to 8/10/2004.

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. Goccia Umbra S.N.C.'s FEI number is 1000409065.

What types of violations has Goccia Umbra S.N.C. received?

Goccia Umbra S.N.C. 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 Goccia Umbra S.N.C. come from?

All FDA import refusal data for Goccia Umbra S.N.C. 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.