Europeenne Decommercialisation
⚠️ Moderate Risk
FEI: 1000230155 • Marseille, Bouches du Rhone • FRANCE
FEI Number
1000230155
Location
Marseille, Bouches du Rhone
Country
FRANCEAddress
2 boulevard Guey, , Marseille, Bouches du Rhone, France
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
UNDER PRC
The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
Frequently Asked Questions
What is Europeenne Decommercialisation's FDA import refusal history?
Europeenne Decommercialisation (FEI: 1000230155) has 2 FDA import refusal record(s) in our database, spanning from 2/21/2002 to 1/29/2004.
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. Europeenne Decommercialisation's FEI number is 1000230155.
What types of violations has Europeenne Decommercialisation received?
Europeenne Decommercialisation 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 Europeenne Decommercialisation come from?
All FDA import refusal data for Europeenne Decommercialisation 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.