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Ahaus GmbH

⚠️ Moderate Risk

FEI: 3004871320 • Huven, Lower Saxony • GERMANY

FEI

FEI Number

3004871320

📍

Location

Huven, Lower Saxony

🇩🇪

Country

GERMANY
🏢

Address

Ahaus Gmbh, Sogeler Str. 3, Huven, Lower Saxony, Germany

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/5/2008
Latest Refusal
9/5/2008
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

Refusal History

DateProductViolationsDivision
9/5/2008
03AGT99BREAD/ROLLS/BUNS, N.E.C.
320LACKS FIRM
3300ALLERGEN
New England District Office (NWE-DO)

Frequently Asked Questions

What is Ahaus GmbH's FDA import refusal history?

Ahaus GmbH (FEI: 3004871320) has 1 FDA import refusal record(s) in our database, spanning from 9/5/2008 to 9/5/2008.

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. Ahaus GmbH's FEI number is 3004871320.

What types of violations has Ahaus GmbH received?

Ahaus GmbH has been cited for 2 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 Ahaus GmbH come from?

All FDA import refusal data for Ahaus 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.