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Solvay Pharmaceuticals

⚠️ Moderate Risk

FEI: 3003060412 • Suresnes, Hauts de Seine • FRANCE

FEI

FEI Number

3003060412

📍

Location

Suresnes, Hauts de Seine

🇫🇷

Country

FRANCE
🏢

Address

42 rue Rouget de Lisle, BP 22, Suresnes, Hauts de Seine, France

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
6/22/2009
Latest Refusal
12/9/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
4.4×10%
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

711×

NO LICENSE

The article is subject to refusal of admission under section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it appears to be a biological product for which a biologics license is not in effect under the Public Health Service Act, Part F, Subpart 1-Biological Products, Section 351(a), and it is not the subject of an Investigational New Drug application that is in effect. Therefore, it appears to be a new drug under 201(p) of the FD&C Act that it is in violation of section 505(a) of the FD&C Act because it lacks a new drug approval and because it is misbranded under section 502(f)(1)of the FD&C Act because it fails to bear adequate directions for use

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
6/22/2009
61JCA09FENOFIBRATE (ANTI-CHOLESTEREMIC)
75UNAPPROVED
New York District Office (NYK-DO)
12/9/2004
57CD02INFLUENZA VIRUS VACCINE
71NO LICENSE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Solvay Pharmaceuticals's FDA import refusal history?

Solvay Pharmaceuticals (FEI: 3003060412) has 2 FDA import refusal record(s) in our database, spanning from 12/9/2004 to 6/22/2009.

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. Solvay Pharmaceuticals's FEI number is 3003060412.

What types of violations has Solvay Pharmaceuticals received?

Solvay Pharmaceuticals has been cited for 2 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 Solvay Pharmaceuticals come from?

All FDA import refusal data for Solvay Pharmaceuticals 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.