ImportRefusal LogoImportRefusal

Medion Ag

⚠️ Moderate Risk

FEI: 3004119480 • Mulheim an der Ruhr, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3004119480

📍

Location

Mulheim an der Ruhr, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Freiherr-vom-Stein-Str. 131, , Mulheim an der Ruhr, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/13/2004
Latest Refusal
12/13/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
12/13/2004
82LKLALPHA-1-ACID-GLYCOPROTEIN, ANTIGEN, ANTISERUM, CONTROL
237NO PMA
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Medion Ag's FDA import refusal history?

Medion Ag (FEI: 3004119480) has 1 FDA import refusal record(s) in our database, spanning from 12/13/2004 to 12/13/2004.

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. Medion Ag's FEI number is 3004119480.

What types of violations has Medion Ag received?

Medion Ag 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 Medion Ag come from?

All FDA import refusal data for Medion Ag 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.