Biomet Merck Belgium
⚠️ Moderate Risk
FEI: 3002856659 • Wilrijk • BELGIUM
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/2/2002 | 87MRYAPPLIANCES AND ACCESSORIES, FIXATION, BONE, ABSORBABLE SINGLE/MULTIPLE COMPONENT | 508NO 510(K) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Biomet Merck Belgium's FDA import refusal history?
Biomet Merck Belgium (FEI: 3002856659) has 1 FDA import refusal record(s) in our database, spanning from 10/2/2002 to 10/2/2002.
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. Biomet Merck Belgium's FEI number is 3002856659.
What types of violations has Biomet Merck Belgium received?
Biomet Merck Belgium 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 Biomet Merck Belgium come from?
All FDA import refusal data for Biomet Merck Belgium 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.