ImportRefusal LogoImportRefusal

Dupont Electronic Materials Inc

⚠️ Moderate Risk

FEI: 1000404869 • Manati, PR • UNITED STATES

FEI

FEI Number

1000404869

📍

Location

Manati, PR

🇺🇸
🏢

Address

PO Box 30200, , Manati, PR, United States

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
7/26/2003
Latest Refusal
7/3/2003
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1792×

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
7/26/2003
60LCP37NALBUPHINE HCL (ANALGESIC)
179AGR RX
Seattle District Office (SEA-DO)
7/3/2003
60LCY99ANALGESIC, N.E.C.
179AGR RX
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Dupont Electronic Materials Inc's FDA import refusal history?

Dupont Electronic Materials Inc (FEI: 1000404869) has 2 FDA import refusal record(s) in our database, spanning from 7/3/2003 to 7/26/2003.

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. Dupont Electronic Materials Inc's FEI number is 1000404869.

What types of violations has Dupont Electronic Materials Inc received?

Dupont Electronic Materials Inc 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 Dupont Electronic Materials Inc come from?

All FDA import refusal data for Dupont Electronic Materials Inc 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.