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Gueldenkron Fruchtsaft GmbH

⚠️ High Risk

FEI: 3004650357 • Nistertal, Rhineland-Palatinate • GERMANY

FEI

FEI Number

3004650357

📍

Location

Nistertal, Rhineland-Palatinate

🇩🇪

Country

GERMANY
🏢

Address

Bruckenstr. 9, , Nistertal, Rhineland-Palatinate, Germany

High Risk

FDA Import Risk Assessment

58.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
11/24/2025
Latest Refusal
11/17/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
97.4×20%
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

38982×

INADPRCCTL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate process controls.

Refusal History

DateProductViolationsDivision
11/24/2025
31GGT01COFFEE DRINK
3898INADPRCCTL
Division of Northeast Imports (DNEI)
11/17/2025
31GGT01COFFEE DRINK
3898INADPRCCTL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Gueldenkron Fruchtsaft GmbH's FDA import refusal history?

Gueldenkron Fruchtsaft GmbH (FEI: 3004650357) has 2 FDA import refusal record(s) in our database, spanning from 11/17/2025 to 11/24/2025.

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. Gueldenkron Fruchtsaft GmbH's FEI number is 3004650357.

What types of violations has Gueldenkron Fruchtsaft GmbH received?

Gueldenkron Fruchtsaft GmbH 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 Gueldenkron Fruchtsaft GmbH come from?

All FDA import refusal data for Gueldenkron Fruchtsaft GmbH 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.