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Laboratoire Dr Paul et Karin Herzog

⚠️ Moderate Risk

FEI: 3007846630 • Lutry, Vaud • SWITZERLAND

FEI

FEI Number

3007846630

📍

Location

Lutry, Vaud

🇨🇭
🏢

Address

Route de Taillepied 1, , Lutry, Vaud, 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
4/3/2008
Latest Refusal
4/3/2008
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
4/3/2008
53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
197COSM COLOR
475COSMETLBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Laboratoire Dr Paul et Karin Herzog's FDA import refusal history?

Laboratoire Dr Paul et Karin Herzog (FEI: 3007846630) has 1 FDA import refusal record(s) in our database, spanning from 4/3/2008 to 4/3/2008.

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. Laboratoire Dr Paul et Karin Herzog's FEI number is 3007846630.

What types of violations has Laboratoire Dr Paul et Karin Herzog received?

Laboratoire Dr Paul et Karin Herzog 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 Laboratoire Dr Paul et Karin Herzog come from?

All FDA import refusal data for Laboratoire Dr Paul et Karin Herzog 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.