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Prod. De Consumo Electronico Philips Sa

⚠️ Moderate Risk

FEI: 3001019655 • Ciudad Ciudad Juarez, Durango • MEXICO

FEI

FEI Number

3001019655

📍

Location

Ciudad Ciudad Juarez, Durango

🇲🇽

Country

MEXICO
🏢

Address

Pqe. Ind. Gema, Apdo. Postal 1698, Lerdo, Ciudad Ciudad Juarez, Durango, Mexico

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
12/1/2004
Latest Refusal
12/1/2004
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
12/1/2004
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
476NO REGISTR
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Prod. De Consumo Electronico Philips Sa's FDA import refusal history?

Prod. De Consumo Electronico Philips Sa (FEI: 3001019655) has 1 FDA import refusal record(s) in our database, spanning from 12/1/2004 to 12/1/2004.

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. Prod. De Consumo Electronico Philips Sa's FEI number is 3001019655.

What types of violations has Prod. De Consumo Electronico Philips Sa received?

Prod. De Consumo Electronico Philips Sa 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 Prod. De Consumo Electronico Philips Sa come from?

All FDA import refusal data for Prod. De Consumo Electronico Philips Sa 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.