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Dermopatch

✅ Low Risk

FEI: 3004641763 • Milan, Milan • ITALY

FEI

FEI Number

3004641763

📍

Location

Milan, Milan

🇮🇹

Country

ITALY
🏢

Address

Via Pietro Redaelli 11, , Milan, Milan, Italy

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
10/17/2004
Latest Refusal
10/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

Refusal History

DateProductViolationsDivision
10/17/2004
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
118NOT LISTED
483DRUG NAME
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dermopatch's FDA import refusal history?

Dermopatch (FEI: 3004641763) has 1 FDA import refusal record(s) in our database, spanning from 10/17/2004 to 10/17/2004.

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. Dermopatch's FEI number is 3004641763.

What types of violations has Dermopatch received?

Dermopatch 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 Dermopatch come from?

All FDA import refusal data for Dermopatch 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.