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Ecm

⚠️ Moderate Risk

FEI: 3003638019 • Angouleme • FRANCE

FEI

FEI Number

3003638019

📍

Location

Angouleme

🇫🇷

Country

FRANCE
🏢

Address

126 Bd De La Republique, , Angouleme, , France

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
3/12/2003
Latest Refusal
5/21/2002
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
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

4762×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
3/12/2003
85HEMIMAGER, ULTRASONIC OBSTETRIC-GYNECOLOGIC
508NO 510(K)
New Orleans District Office (NOL-DO)
5/21/2002
77LWIULTRASOUND, SINUS
476NO REGISTR
New Orleans District Office (NOL-DO)
5/21/2002
77LWIULTRASOUND, SINUS
476NO REGISTR
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ecm's FDA import refusal history?

Ecm (FEI: 3003638019) has 3 FDA import refusal record(s) in our database, spanning from 5/21/2002 to 3/12/2003.

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. Ecm's FEI number is 3003638019.

What types of violations has Ecm received?

Ecm 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 Ecm come from?

All FDA import refusal data for Ecm 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.