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Wolfgang Meiners Medizintechnik GmbH

Low Risk

FEI: 1000225195 • Dusseldorf, Nordrhein-Westfalen • GERMANY

FEI

FEI Number

1000225195

📍

Location

Dusseldorf, Nordrhein-Westfalen

🇩🇪

Country

GERMANY
🏢

Address

Niederstr. 87, , Dusseldorf, Nordrhein-Westfalen, Germany

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/13/2018
Latest Refusal
8/13/2018
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
8/13/2018
74DWZDEVICE, BIOPSY, ENDOMYOCARDIAL
118NOT LISTED
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Wolfgang Meiners Medizintechnik GmbH's FDA import refusal history?

Wolfgang Meiners Medizintechnik GmbH (FEI: 1000225195) has 1 FDA import refusal record(s) in our database, spanning from 8/13/2018 to 8/13/2018.

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. Wolfgang Meiners Medizintechnik GmbH's FEI number is 1000225195.

What types of violations has Wolfgang Meiners Medizintechnik GmbH received?

Wolfgang Meiners Medizintechnik GmbH 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 Wolfgang Meiners Medizintechnik GmbH come from?

All FDA import refusal data for Wolfgang Meiners Medizintechnik 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.