SCPP PLAN DE AYUTLA SC DE RL
⚠️ Moderate Risk
FEI: 3013890873 • Heroica Matamoros, Tamaulipas • MEXICO
FEI Number
3013890873
Location
Heroica Matamoros, Tamaulipas
Country
MEXICOAddress
Calle Dos Altos Lucero 500, Col. Lucero, Matamoros, Heroica Matamoros, Tamaulipas, 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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/30/2003 | 16AFT47WEAKFISH (SEA TROUT) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is SCPP PLAN DE AYUTLA SC DE RL's FDA import refusal history?
SCPP PLAN DE AYUTLA SC DE RL (FEI: 3013890873) has 1 FDA import refusal record(s) in our database, spanning from 9/30/2003 to 9/30/2003.
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. SCPP PLAN DE AYUTLA SC DE RL's FEI number is 3013890873.
What types of violations has SCPP PLAN DE AYUTLA SC DE RL received?
SCPP PLAN DE AYUTLA SC DE RL 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 SCPP PLAN DE AYUTLA SC DE RL come from?
All FDA import refusal data for SCPP PLAN DE AYUTLA SC DE RL 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.