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Dupont de Nemours, E I & Company

⚠️ Moderate Risk

FEI: 2515407 • Wilmington, DE • UNITED STATES

FEI

FEI Number

2515407

📍

Location

Wilmington, DE

🇺🇸
🏢

Address

1007 Market St, Comm Service Bldg., Csb6613c, Wilmington, DE, United States

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/21/2008
Latest Refusal
12/21/2008
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

751×

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
12/21/2008
62OCA41LOSARTAN POTASSIUM (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dupont de Nemours, E I & Company's FDA import refusal history?

Dupont de Nemours, E I & Company (FEI: 2515407) has 1 FDA import refusal record(s) in our database, spanning from 12/21/2008 to 12/21/2008.

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 de Nemours, E I & Company's FEI number is 2515407.

What types of violations has Dupont de Nemours, E I & Company received?

Dupont de Nemours, E I & Company 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 de Nemours, E I & Company come from?

All FDA import refusal data for Dupont de Nemours, E I & Company 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.