Eurofarma Labs
⚠️ High Risk
FEI: 3007119493 • Sao Paulo, Sao Paulo • BRAZIL
FEI Number
3007119493
Location
Sao Paulo, Sao Paulo
Country
BRAZILAddress
Avenida Vereador Jose Diniz 3465, , Sao Paulo, Sao Paulo, Brazil
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is Eurofarma Labs's FDA import refusal history?
Eurofarma Labs (FEI: 3007119493) has 2 FDA import refusal record(s) in our database, spanning from 6/30/2025 to 6/30/2025.
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. Eurofarma Labs's FEI number is 3007119493.
What types of violations has Eurofarma Labs received?
Eurofarma Labs 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 Eurofarma Labs come from?
All FDA import refusal data for Eurofarma Labs 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.