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WALBERG GMBH

⚠️ Moderate Risk

FEI: 3029732139 • Grunwald, Bavaria • GERMANY

FEI

FEI Number

3029732139

📍

Location

Grunwald, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Sudliche Munchner Str. 10b, , Grunwald, Bavaria, Germany

Moderate Risk

FDA Import Risk Assessment

29.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
12/11/2023
Latest Refusal
12/7/2023
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
17.7×30%
Recency
43.0×20%
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

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

4711×

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
12/11/2023
53CD14EYELASH AND EYEBROW TREATMENTS-GEL, OIL, PRIMER, CONDITIONERS, SERUM, FORTIFIERS (EYE MAKEUP PREPARA
3260NO ENGLISH
Division of Southeast Imports (DSEI)
12/7/2023
53CY99OTHER EYE MAKEUP PREPARATIONS, N.E.C.
471CSTIC LBLG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is WALBERG GMBH's FDA import refusal history?

WALBERG GMBH (FEI: 3029732139) has 2 FDA import refusal record(s) in our database, spanning from 12/7/2023 to 12/11/2023.

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. WALBERG GMBH's FEI number is 3029732139.

What types of violations has WALBERG GMBH received?

WALBERG 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 WALBERG GMBH come from?

All FDA import refusal data for WALBERG 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.