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Advanced Microderm

⚠️ Moderate Risk

FEI: 3005761517 • Schaumburg, IL • UNITED STATES

FEI

FEI Number

3005761517

📍

Location

Schaumburg, IL

🇺🇸
🏢

Address

904 S Roselle Rd Pmb 302, , Schaumburg, IL, United States

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/14/2008
Latest Refusal
2/14/2008
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3441×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

Refusal History

DateProductViolationsDivision
2/14/2008
65RAR18SODIUM BICARBONATE (REPLENISHER)
344WARNINGS
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Advanced Microderm's FDA import refusal history?

Advanced Microderm (FEI: 3005761517) has 1 FDA import refusal record(s) in our database, spanning from 2/14/2008 to 2/14/2008.

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. Advanced Microderm's FEI number is 3005761517.

What types of violations has Advanced Microderm received?

Advanced Microderm 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 Advanced Microderm come from?

All FDA import refusal data for Advanced Microderm 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.