Sabina Zilberman
⚠️ Moderate Risk
FEI: 3005838155 • Middlesex • UNITED KINGDOM
FEI Number
3005838155
Location
Middlesex
Country
UNITED KINGDOMAddress
Flat 2, 11 Cambridge Park, , Middlesex, , United Kingdom
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
TISSUE
This human cell, tissue, and cellular and tissue-based product is in violation of Section 361 of the Public Health Service Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/10/2006 | 57KY01SEMEN (SPERM) | 478TISSUE | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Sabina Zilberman's FDA import refusal history?
Sabina Zilberman (FEI: 3005838155) has 1 FDA import refusal record(s) in our database, spanning from 8/10/2006 to 8/10/2006.
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. Sabina Zilberman's FEI number is 3005838155.
What types of violations has Sabina Zilberman received?
Sabina Zilberman 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 Sabina Zilberman come from?
All FDA import refusal data for Sabina Zilberman 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.