ImportRefusal LogoImportRefusal

Filippos Sa

⚠️ Moderate Risk

FEI: 3003328189 • Veroia • GREECE

FEI

FEI Number

3003328189

📍

Location

Veroia

🇬🇷

Country

GREECE
🏢

Address

22, , Veroia, , Greece

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
5/14/2003
Latest Refusal
9/19/2002
Earliest Refusal

Score Breakdown

Violation Severity
95.0×40%
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

1571×

FOREIGN OB

The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
5/14/2003
21GEE13PEACH (PIT FRUIT)
157FOREIGN OB
New England District Office (NWE-DO)
9/19/2002
21GET13PEACH (PIT FRUIT)
249FILTHY
New England District Office (NWE-DO)

Frequently Asked Questions

What is Filippos Sa's FDA import refusal history?

Filippos Sa (FEI: 3003328189) has 2 FDA import refusal record(s) in our database, spanning from 9/19/2002 to 5/14/2003.

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. Filippos Sa's FEI number is 3003328189.

What types of violations has Filippos Sa received?

Filippos Sa has been cited for 2 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 Filippos Sa come from?

All FDA import refusal data for Filippos Sa 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.