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Silesia Gerhard Hanke GmbH & Co. KG

⚠️ Moderate Risk

FEI: 3010007891 • Neuss, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3010007891

📍

Location

Neuss, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Am Alten Bach 20-24, , Neuss, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/20/2012
Latest Refusal
6/20/2012
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3061×

INSANITARY

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.

Refusal History

DateProductViolationsDivision
6/20/2012
28NCT99RAW MATERIAL FOR EXTRACTS AND FLAVORS, N.E.C.
306INSANITARY
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Silesia Gerhard Hanke GmbH & Co. KG's FDA import refusal history?

Silesia Gerhard Hanke GmbH & Co. KG (FEI: 3010007891) has 1 FDA import refusal record(s) in our database, spanning from 6/20/2012 to 6/20/2012.

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. Silesia Gerhard Hanke GmbH & Co. KG's FEI number is 3010007891.

What types of violations has Silesia Gerhard Hanke GmbH & Co. KG received?

Silesia Gerhard Hanke GmbH & Co. KG 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 Silesia Gerhard Hanke GmbH & Co. KG come from?

All FDA import refusal data for Silesia Gerhard Hanke GmbH & Co. KG 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.