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SANOFI-AVENTIS

⚠️ Moderate Risk

FEI: 3013961923 • Sao Paulo • BRAZIL

FEI

FEI Number

3013961923

📍

Location

Sao Paulo

🇧🇷

Country

BRAZIL
🏢

Address

Complexo Parque Da Cida, , Sao Paulo, , Brazil

Moderate Risk

FDA Import Risk Assessment

46.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
3/20/2023
Latest Refusal
3/20/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
29.7×20%
Frequency
10.0×10%
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

751×

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

DateProductViolationsDivision
3/20/2023
65QAY24ORPHENADRINE CITRATE (RELAXANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SANOFI-AVENTIS's FDA import refusal history?

SANOFI-AVENTIS (FEI: 3013961923) has 1 FDA import refusal record(s) in our database, spanning from 3/20/2023 to 3/20/2023.

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. SANOFI-AVENTIS's FEI number is 3013961923.

What types of violations has SANOFI-AVENTIS received?

SANOFI-AVENTIS 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 SANOFI-AVENTIS come from?

All FDA import refusal data for SANOFI-AVENTIS 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.