Marcelo Futerman
⚠️ Moderate Risk
FEI: 3005958802 • Santa Fe • ARGENTINA
FEI Number
3005958802
Location
Santa Fe
Country
ARGENTINAAddress
Cuit Nro 20-14975884-5, , Santa Fe, , Argentina
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
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/15/2010 | 53LC99OTHER SKIN CARE PREPARATIONS, N.E.C. | 474COSMETLBLG | New Orleans District Office (NOL-DO) |
| 3/15/2010 | 53LC99OTHER SKIN CARE PREPARATIONS, N.E.C. | 474COSMETLBLG | New Orleans District Office (NOL-DO) |
| 3/18/2008 | 53LC99OTHER SKIN CARE PREPARATIONS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 3/18/2008 | 53LC99OTHER SKIN CARE PREPARATIONS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 3/13/2008 | 53LC99OTHER SKIN CARE PREPARATIONS, N.E.C. | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Marcelo Futerman's FDA import refusal history?
Marcelo Futerman (FEI: 3005958802) has 5 FDA import refusal record(s) in our database, spanning from 3/13/2008 to 3/15/2010.
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. Marcelo Futerman's FEI number is 3005958802.
What types of violations has Marcelo Futerman received?
Marcelo Futerman has been cited for 3 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 Marcelo Futerman come from?
All FDA import refusal data for Marcelo Futerman 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.