REDOX PHARMA
⚠️ High Risk
FEI: 3026081000 • Vadodara City • INDIA
FEI Number
3026081000
Location
Vadodara City
Country
INDIAAddress
4th Floor Office No 73 Sumeru, Citymall Opp. Krishna Towm Ship, Vadodara City, , India
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 REDOX PHARMA's FDA import refusal history?
REDOX PHARMA (FEI: 3026081000) has 3 FDA import refusal record(s) in our database, spanning from 3/3/2023 to 3/3/2023.
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. REDOX PHARMA's FEI number is 3026081000.
What types of violations has REDOX PHARMA received?
REDOX PHARMA 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 REDOX PHARMA come from?
All FDA import refusal data for REDOX PHARMA 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.