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AEON GMBH

⚠️ Moderate Risk

FEI: 3020220826 • Friedrichsdorf • GERMANY

FEI

FEI Number

3020220826

📍

Location

Friedrichsdorf

🇩🇪

Country

GERMANY
🏢

Address

Benzstr. 13, , Friedrichsdorf, , Germany

Moderate Risk

FDA Import Risk Assessment

38.4
LowModerateHighCritical

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

Statistics

12
Total Refusals
2
Unique Violations
7/13/2022
Latest Refusal
7/13/2022
Earliest Refusal

Score Breakdown

Violation Severity
25.0×40%
Refusal Volume
41.3×30%
Recency
30.0×20%
Frequency
100.0×10%
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

385112×

TPLACKFIRM

This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.

385412×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

Refusal History

DateProductViolationsDivision
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/13/2022
98LAA03E-HOOKAH
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is AEON GMBH's FDA import refusal history?

AEON GMBH (FEI: 3020220826) has 12 FDA import refusal record(s) in our database, spanning from 7/13/2022 to 7/13/2022.

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. AEON GMBH's FEI number is 3020220826.

What types of violations has AEON GMBH received?

AEON 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 AEON GMBH come from?

All FDA import refusal data for AEON 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.