Laboratoires Galderma
⚠️ High Risk
FEI: 3003780659 • Alby Sur Cheran, Auvergne Rhone Alpes • FRANCE
FEI Number
3003780659
Location
Alby Sur Cheran, Auvergne Rhone Alpes
Country
FRANCEAddress
Zone Industrielle Montdesir, , Alby Sur Cheran, Auvergne Rhone Alpes, France
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/22/2025 | 62LDY47IVERMECTIN (ANTI-PROTOZOAL, A-LEISHMANIAL, ANTI-MALARIAL) | Division of Southeast Imports (DSEI) | |
| 1/22/2025 | 62LDO40METRONIDAZOLE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL) | Division of Southeast Imports (DSEI) | |
| 5/6/2019 | 62SDO02ADAPALENE (ANTI-SEBORRHEIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Laboratoires Galderma's FDA import refusal history?
Laboratoires Galderma (FEI: 3003780659) has 3 FDA import refusal record(s) in our database, spanning from 5/6/2019 to 1/22/2025.
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 Galderma's FEI number is 3003780659.
What types of violations has Laboratoires Galderma received?
Laboratoires Galderma 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 Laboratoires Galderma come from?
All FDA import refusal data for Laboratoires Galderma 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.