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Mondi Lamex

⚠️ High Risk

FEI: 3011124011 • Vrdila, Kraljevo • SERBIA

FEI

FEI Number

3011124011

📍

Location

Vrdila, Kraljevo

🇷🇸

Country

SERBIA
🏢

Address

Kralja Milana 117, , Vrdila, Kraljevo, Serbia

High Risk

FDA Import Risk Assessment

57.6
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
6/30/2022
Latest Refusal
2/23/2022
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
29.3×20%
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

2414×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
6/30/2022
20AGD13RASPBERRIES, RED (BERRY)
241PESTICIDE
Division of West Coast Imports (DWCI)
6/21/2022
20AGD13RASPBERRIES, RED (BERRY)
241PESTICIDE
Division of Southeast Imports (DSEI)
5/27/2022
20AGD13RASPBERRIES, RED (BERRY)
241PESTICIDE
Division of Northern Border Imports (DNBI)
2/23/2022
20AGD13RASPBERRIES, RED (BERRY)
241PESTICIDE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Mondi Lamex's FDA import refusal history?

Mondi Lamex (FEI: 3011124011) has 4 FDA import refusal record(s) in our database, spanning from 2/23/2022 to 6/30/2022.

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. Mondi Lamex's FEI number is 3011124011.

What types of violations has Mondi Lamex received?

Mondi Lamex 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 Mondi Lamex come from?

All FDA import refusal data for Mondi Lamex 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.