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Mediconsult Gmbh

⚠️ Moderate Risk

FEI: 3007242556 • Dulliken, Solothurn • SWITZERLAND

FEI

FEI Number

3007242556

📍

Location

Dulliken, Solothurn

🇨🇭
🏢

Address

Bodenackerstrasse 69, , Dulliken, Solothurn, Switzerland

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/5/2009
Latest Refusal
12/5/2009
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
12/5/2009
53LC02DEPILATORIES (SKIN CARE PREPARATIONS)
197COSM COLOR
475COSMETLBLG
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Mediconsult Gmbh's FDA import refusal history?

Mediconsult Gmbh (FEI: 3007242556) has 1 FDA import refusal record(s) in our database, spanning from 12/5/2009 to 12/5/2009.

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. Mediconsult Gmbh's FEI number is 3007242556.

What types of violations has Mediconsult Gmbh received?

Mediconsult 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 Mediconsult Gmbh come from?

All FDA import refusal data for Mediconsult 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.