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Medit Gmbh

⚠️ Moderate Risk

FEI: 3003172449 • Pottmes, Bavaria • GERMANY

FEI

FEI Number

3003172449

📍

Location

Pottmes, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Ebenried 65, , Pottmes, Bavaria, Germany

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
7/27/2012
Latest Refusal
9/22/2003
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.4×10%
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

1182×

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
7/27/2012
87KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
473LABELING
New Orleans District Office (NOL-DO)
9/22/2003
79GEHUNIT, CRYOSURGICAL, ACCESSORIES
118NOT LISTED
New Orleans District Office (NOL-DO)
9/22/2003
87HRXARTHROSCOPE AND ACCESSORIES
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Medit Gmbh's FDA import refusal history?

Medit Gmbh (FEI: 3003172449) has 3 FDA import refusal record(s) in our database, spanning from 9/22/2003 to 7/27/2012.

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. Medit Gmbh's FEI number is 3003172449.

What types of violations has Medit Gmbh received?

Medit 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 Medit Gmbh come from?

All FDA import refusal data for Medit 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.