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CENTRALE FILLERS

⚠️ High Risk

FEI: 3023212124 • Montpellier, Herault • FRANCE

FEI

FEI Number

3023212124

📍

Location

Montpellier, Herault

🇫🇷

Country

FRANCE
🏢

Address

73 Allee Kleber, , Montpellier, Herault, France

High Risk

FDA Import Risk Assessment

50.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
11/22/2023
Latest Refusal
11/22/2023
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
57.3×20%
Frequency
20.0×10%
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

3422×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

752×

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
11/22/2023
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
342PERSONALRX
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/22/2023
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
342PERSONALRX
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is CENTRALE FILLERS's FDA import refusal history?

CENTRALE FILLERS (FEI: 3023212124) has 2 FDA import refusal record(s) in our database, spanning from 11/22/2023 to 11/22/2023.

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. CENTRALE FILLERS's FEI number is 3023212124.

What types of violations has CENTRALE FILLERS received?

CENTRALE FILLERS 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 CENTRALE FILLERS come from?

All FDA import refusal data for CENTRALE FILLERS 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.