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S. Goldmann Gmbh & Co. Kg

⚠️ Moderate Risk

FEI: 3007639170 • Bielefeld, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3007639170

📍

Location

Bielefeld, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Schillerstr. 79, , Bielefeld, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/7/2009
Latest Refusal
8/7/2009
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1972×

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).

Refusal History

DateProductViolationsDivision
8/7/2009
50JGH99CERT. COLORS FOR USE IN COSMETICS ONLY, N.E.C.
197COSM COLOR
San Francisco District Office (SAN-DO)
8/7/2009
50JGH99CERT. COLORS FOR USE IN COSMETICS ONLY, N.E.C.
197COSM COLOR
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is S. Goldmann Gmbh & Co. Kg's FDA import refusal history?

S. Goldmann Gmbh & Co. Kg (FEI: 3007639170) has 2 FDA import refusal record(s) in our database, spanning from 8/7/2009 to 8/7/2009.

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. S. Goldmann Gmbh & Co. Kg's FEI number is 3007639170.

What types of violations has S. Goldmann Gmbh & Co. Kg received?

S. Goldmann Gmbh & Co. Kg has been cited for 1 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 S. Goldmann Gmbh & Co. Kg come from?

All FDA import refusal data for S. Goldmann Gmbh & Co. Kg 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.