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Hans Munzinger Chirurgische Instrumente

✅ Low Risk

FEI: 1000182785 • Tuttlingen, Baden-Wurttemberg • GERMANY

FEI

FEI Number

1000182785

📍

Location

Tuttlingen, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Lohmehlenring 108, , Tuttlingen, Baden-Wurttemberg, Germany

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/20/2001
Latest Refusal
11/20/2001
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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).

Refusal History

DateProductViolationsDivision
11/20/2001
79MDMINSTRUMENT, MANUAL, GENERAL SURGICAL
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Hans Munzinger Chirurgische Instrumente's FDA import refusal history?

Hans Munzinger Chirurgische Instrumente (FEI: 1000182785) has 1 FDA import refusal record(s) in our database, spanning from 11/20/2001 to 11/20/2001.

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. Hans Munzinger Chirurgische Instrumente's FEI number is 1000182785.

What types of violations has Hans Munzinger Chirurgische Instrumente received?

Hans Munzinger Chirurgische Instrumente 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 Hans Munzinger Chirurgische Instrumente come from?

All FDA import refusal data for Hans Munzinger Chirurgische Instrumente 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.