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KSE PROCESS TECHNOLOGY

⚠️ Moderate Risk

FEI: 3015338551 • Bladel, Noord-Brabant • NETHERLANDS

FEI

FEI Number

3015338551

📍

Location

Bladel, Noord-Brabant

🇳🇱
🏢

Address

Rondweg 27, , Bladel, Noord-Brabant, Netherlands

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
5/24/2019
Latest Refusal
5/24/2019
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

4761×

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
5/24/2019
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is KSE PROCESS TECHNOLOGY's FDA import refusal history?

KSE PROCESS TECHNOLOGY (FEI: 3015338551) has 1 FDA import refusal record(s) in our database, spanning from 5/24/2019 to 5/24/2019.

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. KSE PROCESS TECHNOLOGY's FEI number is 3015338551.

What types of violations has KSE PROCESS TECHNOLOGY received?

KSE PROCESS TECHNOLOGY 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 KSE PROCESS TECHNOLOGY come from?

All FDA import refusal data for KSE PROCESS TECHNOLOGY 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.