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Ethex Corp

⚠️ Moderate Risk

FEI: 3002896610 • Bridgeton, MO • UNITED STATES

FEI

FEI Number

3002896610

📍

Location

Bridgeton, MO

🇺🇸
🏢

Address

#1 Corporate Woods, , Bridgeton, MO, United States

Moderate Risk

FDA Import Risk Assessment

36.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
8/21/2009
Latest Refusal
2/1/2007
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
7.8×10%
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

1791×

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.

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
8/21/2009
62ODA14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
179AGR RX
Southwest Import District Office (SWI-DO)
2/1/2007
62OAP27DOXAZOSIN MESYLATE (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ethex Corp's FDA import refusal history?

Ethex Corp (FEI: 3002896610) has 2 FDA import refusal record(s) in our database, spanning from 2/1/2007 to 8/21/2009.

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. Ethex Corp's FEI number is 3002896610.

What types of violations has Ethex Corp received?

Ethex Corp has been cited for 2 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 Ethex Corp come from?

All FDA import refusal data for Ethex Corp 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.