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Hormocenta Tagescreme

⚠️ Moderate Risk

FEI: 3011124679 • Essen, Nordrhein-westfalen • GERMANY

FEI

FEI Number

3011124679

📍

Location

Essen, Nordrhein-westfalen

🇩🇪

Country

GERMANY
🏢

Address

Am Alfredusbad 2, , Essen, Nordrhein-westfalen, Germany

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
11/13/2014
Latest Refusal
11/13/2014
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4713×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
11/13/2014
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
Cincinnati District Office (CIN-DO)
11/13/2014
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
Cincinnati District Office (CIN-DO)
11/13/2014
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Hormocenta Tagescreme's FDA import refusal history?

Hormocenta Tagescreme (FEI: 3011124679) has 3 FDA import refusal record(s) in our database, spanning from 11/13/2014 to 11/13/2014.

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. Hormocenta Tagescreme's FEI number is 3011124679.

What types of violations has Hormocenta Tagescreme received?

Hormocenta Tagescreme 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 Hormocenta Tagescreme come from?

All FDA import refusal data for Hormocenta Tagescreme 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.