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Standard Instrumen

⚠️ Moderate Risk

FEI: 3007101744 • Karlsruhe, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3007101744

📍

Location

Karlsruhe, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Werftstr. 12, , Karlsruhe, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

42.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/3/2024
Latest Refusal
9/3/2024
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
72.5×20%
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).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
9/3/2024
84HCGDEVICE, ARTIFICIAL EMBOLIZATION
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Standard Instrumen's FDA import refusal history?

Standard Instrumen (FEI: 3007101744) has 1 FDA import refusal record(s) in our database, spanning from 9/3/2024 to 9/3/2024.

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. Standard Instrumen's FEI number is 3007101744.

What types of violations has Standard Instrumen received?

Standard Instrumen 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 Standard Instrumen come from?

All FDA import refusal data for Standard Instrumen 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.