ImportRefusal LogoImportRefusal

Arburg Gmbh & Co

⚠️ Moderate Risk

FEI: 3001072939 • Loburg • GERMANY

FEI

FEI Number

3001072939

📍

Location

Loburg

🇩🇪

Country

GERMANY
🏢

Address

Arthur-Hehl-Strasse, , Loburg, , Germany

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/26/2006
Latest Refusal
10/21/2004
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
10.3×10%
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
9/26/2006
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
476NO REGISTR
New York District Office (NYK-DO)
10/21/2004
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
476NO REGISTR
New York District Office (NYK-DO)

Frequently Asked Questions

What is Arburg Gmbh & Co's FDA import refusal history?

Arburg Gmbh & Co (FEI: 3001072939) has 2 FDA import refusal record(s) in our database, spanning from 10/21/2004 to 9/26/2006.

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. Arburg Gmbh & Co's FEI number is 3001072939.

What types of violations has Arburg Gmbh & Co received?

Arburg Gmbh & Co 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 Arburg Gmbh & Co come from?

All FDA import refusal data for Arburg Gmbh & Co 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.