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Aleva Novi Knezevac

⚠️ High Risk

FEI: 3007046845 • Serbia • SERBIA

FEI

FEI Number

3007046845

📍

Location

Serbia

🇷🇸

Country

SERBIA
🏢

Address

Svetosavski Trg 1 Vrsac, , Serbia, , Serbia

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

4
Total Refusals
1
Unique Violations
7/15/2009
Latest Refusal
7/15/2009
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

94×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
7/15/2009
28BGT33PAPRIKA, GROUND, CRACKED (SPICE)
9SALMONELLA
Detroit District Office (DET-DO)
7/15/2009
28BGT33PAPRIKA, GROUND, CRACKED (SPICE)
9SALMONELLA
Detroit District Office (DET-DO)
7/15/2009
28BGT33PAPRIKA, GROUND, CRACKED (SPICE)
9SALMONELLA
Detroit District Office (DET-DO)
7/15/2009
28BGT33PAPRIKA, GROUND, CRACKED (SPICE)
9SALMONELLA
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Aleva Novi Knezevac's FDA import refusal history?

Aleva Novi Knezevac (FEI: 3007046845) has 4 FDA import refusal record(s) in our database, spanning from 7/15/2009 to 7/15/2009.

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. Aleva Novi Knezevac's FEI number is 3007046845.

What types of violations has Aleva Novi Knezevac received?

Aleva Novi Knezevac 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 Aleva Novi Knezevac come from?

All FDA import refusal data for Aleva Novi Knezevac 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.