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TANIA MARIA MOURA

⚠️ High Risk

FEI: 3030234795 • Rio De Janeiro, Rio de Janeiro • BRAZIL

FEI

FEI Number

3030234795

📍

Location

Rio De Janeiro, Rio de Janeiro

🇧🇷

Country

BRAZIL
🏢

Address

Estrada Da Posse, 3750 Apt 303, , Rio De Janeiro, Rio de Janeiro, Brazil

High Risk

FDA Import Risk Assessment

54.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
1/26/2024
Latest Refusal
1/26/2024
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
46.0×20%
Frequency
30.0×10%
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

753×

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
1/26/2024
61MCY06CLONAZEPAM (ANTI-CONVULSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/26/2024
61NCY29FLUOXETINE (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/26/2024
61NCY05BUPROPION HCL (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TANIA MARIA MOURA's FDA import refusal history?

TANIA MARIA MOURA (FEI: 3030234795) has 3 FDA import refusal record(s) in our database, spanning from 1/26/2024 to 1/26/2024.

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. TANIA MARIA MOURA's FEI number is 3030234795.

What types of violations has TANIA MARIA MOURA received?

TANIA MARIA MOURA 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 TANIA MARIA MOURA come from?

All FDA import refusal data for TANIA MARIA MOURA 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.