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Renaudin

⚠️ Moderate Risk

FEI: 3004495153 • St. Cloud • FRANCE

FEI

FEI Number

3004495153

📍

Location

St. Cloud

🇫🇷

Country

FRANCE
🏢

Address

125 Bureaux De La Colline, , St. Cloud, , France

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/23/2017
Latest Refusal
3/21/2017
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
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
3/23/2017
62LCK37QUININE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
New Orleans District Office (NOL-DO)
3/23/2017
62GCP18DICLOFENAC SODIUM (ANTI-INFLAMMATORY)
75UNAPPROVED
New Orleans District Office (NOL-DO)
3/21/2017
62LCK37QUININE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Renaudin's FDA import refusal history?

Renaudin (FEI: 3004495153) has 3 FDA import refusal record(s) in our database, spanning from 3/21/2017 to 3/23/2017.

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. Renaudin's FEI number is 3004495153.

What types of violations has Renaudin received?

Renaudin 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 Renaudin come from?

All FDA import refusal data for Renaudin 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.