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Phillips Belgium Ltd

✅ Low Risk

FEI: 3008918744 • Anderlecht, Brussels-Capital Region • BELGIUM

FEI

FEI Number

3008918744

📍

Location

Anderlecht, Brussels-Capital Region

🇧🇪

Country

BELGIUM
🏢

Address

Rue De L'Ancienne Gare 80, , Anderlecht, Brussels-Capital Region, Belgium

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
6/27/2013
Latest Refusal
6/27/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
6/27/2013
95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS
126FAILS STD
333LACKS FIRM
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Phillips Belgium Ltd's FDA import refusal history?

Phillips Belgium Ltd (FEI: 3008918744) has 1 FDA import refusal record(s) in our database, spanning from 6/27/2013 to 6/27/2013.

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. Phillips Belgium Ltd's FEI number is 3008918744.

What types of violations has Phillips Belgium Ltd received?

Phillips Belgium Ltd 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 Phillips Belgium Ltd come from?

All FDA import refusal data for Phillips Belgium Ltd 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.