Orval Kent de Linares - Plant 1
⚠️ Moderate Risk
FEI: 1000253286 • Linares, Nuevo Leon • MEXICO
FEI Number
1000253286
Location
Linares, Nuevo Leon
Country
MEXICOAddress
Orval Kent de Linares, S de RL de CV, Belisario Dominguez 900 Ote, Col. ALVARADO, Linares, Nuevo Leon, Mexico
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
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
Frequently Asked Questions
What is Orval Kent de Linares - Plant 1's FDA import refusal history?
Orval Kent de Linares - Plant 1 (FEI: 1000253286) has 1 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 12/3/2002.
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. Orval Kent de Linares - Plant 1's FEI number is 1000253286.
What types of violations has Orval Kent de Linares - Plant 1 received?
Orval Kent de Linares - Plant 1 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 Orval Kent de Linares - Plant 1 come from?
All FDA import refusal data for Orval Kent de Linares - Plant 1 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.