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Laboratoires Filorga S.A.S.

⚠️ Moderate Risk

FEI: 3008263076 • Paris, Paris • FRANCE

FEI

FEI Number

3008263076

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

2 rue de Lisbonne, , Paris, Paris, France

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
7/9/2018
Latest Refusal
7/9/2018
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

24801×

RXPERSONAL

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

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
7/9/2018
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
237NO PMA
2480RXPERSONAL
84RX DEVICE
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Laboratoires Filorga S.A.S.'s FDA import refusal history?

Laboratoires Filorga S.A.S. (FEI: 3008263076) has 1 FDA import refusal record(s) in our database, spanning from 7/9/2018 to 7/9/2018.

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. Laboratoires Filorga S.A.S.'s FEI number is 3008263076.

What types of violations has Laboratoires Filorga S.A.S. received?

Laboratoires Filorga S.A.S. has been cited for 3 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 Laboratoires Filorga S.A.S. come from?

All FDA import refusal data for Laboratoires Filorga S.A.S. 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.