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Pti Advanced Filtration

⚠️ Moderate Risk

FEI: 3003588063 • Oro-Medonte, Ontario • CANADA

FEI

FEI Number

3003588063

📍

Location

Oro-Medonte, Ontario

🇨🇦

Country

CANADA
🏢

Address

Rr #, , Oro-Medonte, Ontario, Canada

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/10/2002
Latest Refusal
5/10/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1793×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
5/10/2002
62OCA28ENALAPRIL MALEATE (ANTI-HYPERTENSIVE - PART II)
179AGR RX
New Orleans District Office (NOL-DO)
5/10/2002
61PCA11GLYBURIDE (ANTI-DIABETIC)
179AGR RX
New Orleans District Office (NOL-DO)
5/10/2002
64BCA25HYDROCHLOROTHIAZIDE (DIURETIC)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Pti Advanced Filtration's FDA import refusal history?

Pti Advanced Filtration (FEI: 3003588063) has 3 FDA import refusal record(s) in our database, spanning from 5/10/2002 to 5/10/2002.

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. Pti Advanced Filtration's FEI number is 3003588063.

What types of violations has Pti Advanced Filtration received?

Pti Advanced Filtration 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 Pti Advanced Filtration come from?

All FDA import refusal data for Pti Advanced Filtration 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.