ImportRefusal LogoImportRefusal

Ferrotron Technologies Gmbh

⚠️ Moderate Risk

FEI: 3003256512 • Moers, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3003256512

📍

Location

Moers, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Am Schurmannshutt 30, , Moers, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
3/25/2003
Latest Refusal
6/6/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

4762×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
3/25/2003
95L22LASER PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
Cincinnati District Office (CIN-DO)
6/6/2002
94V05CATHODE RAY TUBE
476NO REGISTR
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Ferrotron Technologies Gmbh's FDA import refusal history?

Ferrotron Technologies Gmbh (FEI: 3003256512) has 2 FDA import refusal record(s) in our database, spanning from 6/6/2002 to 3/25/2003.

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. Ferrotron Technologies Gmbh's FEI number is 3003256512.

What types of violations has Ferrotron Technologies Gmbh received?

Ferrotron Technologies Gmbh 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 Ferrotron Technologies Gmbh come from?

All FDA import refusal data for Ferrotron Technologies 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.