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I.M. Lehmann Gmbh

✅ Low Risk

FEI: 3004025553 • Welter • GERMANY

FEI

FEI Number

3004025553

📍

Location

Welter

🇩🇪

Country

GERMANY
🏢

Address

Altenhofer Weg 17, , Welter, , Germany

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
2
Unique Violations
8/15/2003
Latest Refusal
8/15/2003
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

4712×

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.

4742×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

Refusal History

DateProductViolationsDivision
8/15/2003
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
474COSMETLBLG
New Orleans District Office (NOL-DO)
8/15/2003
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
474COSMETLBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is I.M. Lehmann Gmbh's FDA import refusal history?

I.M. Lehmann Gmbh (FEI: 3004025553) has 2 FDA import refusal record(s) in our database, spanning from 8/15/2003 to 8/15/2003.

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. I.M. Lehmann Gmbh's FEI number is 3004025553.

What types of violations has I.M. Lehmann Gmbh received?

I.M. Lehmann 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 I.M. Lehmann Gmbh come from?

All FDA import refusal data for I.M. Lehmann 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.