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Erbrich-Instrumente Gmbh

⚠️ Moderate Risk

FEI: 3002806921 • Tuttlingen, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3002806921

📍

Location

Tuttlingen, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Eugenstr. 33, , Tuttlingen, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/15/2003
Latest Refusal
8/14/2002
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
19.9×10%
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).

Refusal History

DateProductViolationsDivision
8/15/2003
77KCBTUBE, TONSIL SUCTION
118NOT LISTED
Chicago District Office (CHI-DO)
8/14/2002
79MDWINSTRUMENT, MANUAL, SURGICAL, GENERAL USE
118NOT LISTED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Erbrich-Instrumente Gmbh's FDA import refusal history?

Erbrich-Instrumente Gmbh (FEI: 3002806921) has 2 FDA import refusal record(s) in our database, spanning from 8/14/2002 to 8/15/2003.

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. Erbrich-Instrumente Gmbh's FEI number is 3002806921.

What types of violations has Erbrich-Instrumente Gmbh received?

Erbrich-Instrumente 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 Erbrich-Instrumente Gmbh come from?

All FDA import refusal data for Erbrich-Instrumente 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.