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Leaderm

⚠️ Moderate Risk

FEI: 3003218448 • Paris, Paris • FRANCE

FEI

FEI Number

3003218448

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

28 rue de Caumartin, , Paris, Paris, France

Moderate Risk

FDA Import Risk Assessment

34.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
3/12/2003
Latest Refusal
3/12/2003
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
3/12/2003
66VDJ99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
27DRUG GMPS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Leaderm's FDA import refusal history?

Leaderm (FEI: 3003218448) has 1 FDA import refusal record(s) in our database, spanning from 3/12/2003 to 3/12/2003.

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. Leaderm's FEI number is 3003218448.

What types of violations has Leaderm received?

Leaderm 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 Leaderm come from?

All FDA import refusal data for Leaderm 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.