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Fr De Luzuriaga

⚠️ Moderate Risk

FEI: 3005051913 • Bacolod City, Negros Island Region • PHILIPPINES

FEI

FEI Number

3005051913

📍

Location

Bacolod City, Negros Island Region

🇵🇭
🏢

Address

5 Tanguile, , Bacolod City, Negros Island Region, Philippines

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/4/2005
Latest Refusal
5/4/2005
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
5/4/2005
61QCA99ANTI-DIURETIC N.E.C.
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/4/2005
66MCA61THIORIDAZINE HCL (TRANQUILIZER)
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/4/2005
62CCA99ANTI-HYPERTENSIVE N.E.C.
75UNAPPROVED
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Fr De Luzuriaga's FDA import refusal history?

Fr De Luzuriaga (FEI: 3005051913) has 3 FDA import refusal record(s) in our database, spanning from 5/4/2005 to 5/4/2005.

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. Fr De Luzuriaga's FEI number is 3005051913.

What types of violations has Fr De Luzuriaga received?

Fr De Luzuriaga 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 Fr De Luzuriaga come from?

All FDA import refusal data for Fr De Luzuriaga 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.