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Saalemuehle Alsleben GmbH

⚠️ Moderate Risk

FEI: 3013220167 • Alsleben (Saale), Saxony-Anhalt • GERMANY

FEI

FEI Number

3013220167

📍

Location

Alsleben (Saale), Saxony-Anhalt

🇩🇪

Country

GERMANY
🏢

Address

Bernburger Str. 35b, , Alsleben (Saale), Saxony-Anhalt, Germany

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
5/12/2020
Latest Refusal
5/12/2020
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

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
5/12/2020
18EFH01CEREAL BASE MEAT EXTENDERS, WHEAT PROTEIN, ETC.
241PESTICIDE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Saalemuehle Alsleben GmbH's FDA import refusal history?

Saalemuehle Alsleben GmbH (FEI: 3013220167) has 1 FDA import refusal record(s) in our database, spanning from 5/12/2020 to 5/12/2020.

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. Saalemuehle Alsleben GmbH's FEI number is 3013220167.

What types of violations has Saalemuehle Alsleben GmbH received?

Saalemuehle Alsleben 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 Saalemuehle Alsleben GmbH come from?

All FDA import refusal data for Saalemuehle Alsleben 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.