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Titania Fabrik GmbH

⚠️ Moderate Risk

FEI: 3009916849 • Wulfrath, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3009916849

📍

Location

Wulfrath, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Fortuna Strasse 10-14, , Wulfrath, North Rhine-Westphalia, Germany

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
3/2/2016
Latest Refusal
3/2/2016
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
3/2/2016
53FD01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
197COSM COLOR
475COSMETLBLG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Titania Fabrik GmbH's FDA import refusal history?

Titania Fabrik GmbH (FEI: 3009916849) has 1 FDA import refusal record(s) in our database, spanning from 3/2/2016 to 3/2/2016.

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. Titania Fabrik GmbH's FEI number is 3009916849.

What types of violations has Titania Fabrik GmbH received?

Titania Fabrik 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 Titania Fabrik GmbH come from?

All FDA import refusal data for Titania Fabrik 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.