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Bruker Axs Gmbh

⚠️ Moderate Risk

FEI: 3002627743 • Karlsruhe, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3002627743

📍

Location

Karlsruhe, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Ostliche Rheinbruckenstr. 50, , Karlsruhe, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
1/13/2023
Latest Refusal
1/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
17.7×30%
Recency
39.7×20%
Frequency
0.9×10%
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

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).

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

Refusal History

DateProductViolationsDivision
1/13/2023
90IZGSYSTEM, X-RAY, PHOTOFLUOROGRAPHIC
476NO REGISTR
Division of Northern Border Imports (DNBI)
1/3/2002
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
47NON STD
476NO REGISTR
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Bruker Axs Gmbh's FDA import refusal history?

Bruker Axs Gmbh (FEI: 3002627743) has 2 FDA import refusal record(s) in our database, spanning from 1/3/2002 to 1/13/2023.

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. Bruker Axs Gmbh's FEI number is 3002627743.

What types of violations has Bruker Axs Gmbh received?

Bruker Axs 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 Bruker Axs Gmbh come from?

All FDA import refusal data for Bruker Axs 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.