Argenmex Sa
✅ Low Risk
FEI: 3002627068 • Ciudad Autonoma Buenos Aires, Capital Federal • ARGENTINA
FEI Number
3002627068
Location
Ciudad Autonoma Buenos Aires, Capital Federal
Country
ARGENTINAAddress
Calle Rivera Indarte 327, , Ciudad Autonoma Buenos Aires, Capital Federal, Argentina
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2002 | 64LCS61TRIAMCINOLONE ACETONIDE (GLUCOCORTICOID) | 2880RXCOMPOUND | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Argenmex Sa's FDA import refusal history?
Argenmex Sa (FEI: 3002627068) has 1 FDA import refusal record(s) in our database, spanning from 11/22/2002 to 11/22/2002.
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. Argenmex Sa's FEI number is 3002627068.
What types of violations has Argenmex Sa received?
Argenmex Sa 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 Argenmex Sa come from?
All FDA import refusal data for Argenmex Sa 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.