Waechil
⚠️ Moderate Risk
FEI: 3001245120 • Condet En Feniers • FRANCE
FEI Number
3001245120
Location
Condet En Feniers
Country
FRANCEAddress
Unknown Street, , Condet En Feniers, , 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
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 |
|---|---|---|---|
| 8/19/2004 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Waechil's FDA import refusal history?
Waechil (FEI: 3001245120) has 1 FDA import refusal record(s) in our database, spanning from 8/19/2004 to 8/19/2004.
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. Waechil's FEI number is 3001245120.
What types of violations has Waechil received?
Waechil 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 Waechil come from?
All FDA import refusal data for Waechil 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.