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Arko Przedsiebiorstwo Handlowe

⚠️ Moderate Risk

FEI: 3003188064 • Poznan, Wielkopolskie • POLAND

FEI

FEI Number

3003188064

📍

Location

Poznan, Wielkopolskie

🇵🇱

Country

POLAND
🏢

Address

Ul. Kaliowa 38, , Poznan, Wielkopolskie, Poland

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/2/2002
Latest Refusal
6/28/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

623×

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
8/2/2002
38YCF99SOUP, N.E.C.
62NEEDS FCE
Chicago District Office (CHI-DO)
8/2/2002
38YCF99SOUP, N.E.C.
62NEEDS FCE
Chicago District Office (CHI-DO)
6/28/2002
38YCF99SOUP, N.E.C.
62NEEDS FCE
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Arko Przedsiebiorstwo Handlowe's FDA import refusal history?

Arko Przedsiebiorstwo Handlowe (FEI: 3003188064) has 3 FDA import refusal record(s) in our database, spanning from 6/28/2002 to 8/2/2002.

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. Arko Przedsiebiorstwo Handlowe's FEI number is 3003188064.

What types of violations has Arko Przedsiebiorstwo Handlowe received?

Arko Przedsiebiorstwo Handlowe 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 Arko Przedsiebiorstwo Handlowe come from?

All FDA import refusal data for Arko Przedsiebiorstwo Handlowe 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.