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Gruppo Bioimpianti Srl

⚠️ Moderate Risk

FEI: 3007391088 • Peschiera Borromeo, Milan • ITALY

FEI

FEI Number

3007391088

📍

Location

Peschiera Borromeo, Milan

🇮🇹

Country

ITALY
🏢

Address

Via Liguria 28, , Peschiera Borromeo, Milan, Italy

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
3/3/2004
Latest Refusal
3/3/2004
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
3/3/2004
87KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
118NOT LISTED
Division of Southeast Imports (DSEI)
3/3/2004
87JDDPROSTHESIS, UPPER FEMORAL
118NOT LISTED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Gruppo Bioimpianti Srl's FDA import refusal history?

Gruppo Bioimpianti Srl (FEI: 3007391088) has 2 FDA import refusal record(s) in our database, spanning from 3/3/2004 to 3/3/2004.

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. Gruppo Bioimpianti Srl's FEI number is 3007391088.

What types of violations has Gruppo Bioimpianti Srl received?

Gruppo Bioimpianti Srl 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 Gruppo Bioimpianti Srl come from?

All FDA import refusal data for Gruppo Bioimpianti Srl 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.