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Smi Equipments

⚠️ Moderate Risk

FEI: 3004192848 • Coignieres, Yvelines • FRANCE

FEI

FEI Number

3004192848

📍

Location

Coignieres, Yvelines

🇫🇷

Country

FRANCE
🏢

Address

29 avenue de la Gare, Bp 23, Coignieres, Yvelines, France

Moderate Risk

FDA Import Risk Assessment

37.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
2/26/2008
Latest Refusal
2/26/2008
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
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

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

5082×

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
2/26/2008
91NEDKIT, TEST, MALARIA,
237NO PMA
508NO 510(K)
Cincinnati District Office (CIN-DO)
2/26/2008
91NEDKIT, TEST, MALARIA,
237NO PMA
508NO 510(K)
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Smi Equipments's FDA import refusal history?

Smi Equipments (FEI: 3004192848) has 2 FDA import refusal record(s) in our database, spanning from 2/26/2008 to 2/26/2008.

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. Smi Equipments's FEI number is 3004192848.

What types of violations has Smi Equipments received?

Smi Equipments 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 Smi Equipments come from?

All FDA import refusal data for Smi Equipments 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.