Rivoire Et Jacquemin
⚠️ High Risk
FEI: 3003631317 • Mortmarot • FRANCE
FEI Number
3003631317
Location
Mortmarot
Country
FRANCEAddress
Unknown Street, , Mortmarot, , 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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/3/2003 | 12AMP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | Minneapolis District Office (MIN-DO) |
| 6/26/2003 | 12CMO16CHEESE, SHEEP, N.E.C. | 295LISTERIA | Minneapolis District Office (MIN-DO) |
| 4/8/2002 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New York District Office (NYK-DO) |
| 4/8/2002 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New York District Office (NYK-DO) |
| 2/5/2002 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Rivoire Et Jacquemin's FDA import refusal history?
Rivoire Et Jacquemin (FEI: 3003631317) has 5 FDA import refusal record(s) in our database, spanning from 2/5/2002 to 12/3/2003.
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. Rivoire Et Jacquemin's FEI number is 3003631317.
What types of violations has Rivoire Et Jacquemin received?
Rivoire Et Jacquemin has been cited for 1 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 Rivoire Et Jacquemin come from?
All FDA import refusal data for Rivoire Et Jacquemin 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.