ACUACULTURA AZTLAN
⚠️ High Risk
FEI: 3008101441 • Tepic, Nayarit • MEXICO
FEI Number
3008101441
Location
Tepic, Nayarit
Country
MEXICOAddress
Calle Adolfo Lopez Mateos No 198, Col. ADOLFO LOPEZ MATEOS, Tepic, Nayarit, Mexico
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
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 |
|---|---|---|---|
| 11/23/2010 | 16JGD05SHRIMP & PRAWNS | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/23/2010 | 16JGD05SHRIMP & PRAWNS | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/23/2010 | 16JGD05SHRIMP & PRAWNS | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/23/2010 | 16JGD05SHRIMP & PRAWNS | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/23/2010 | 16XGD21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is ACUACULTURA AZTLAN's FDA import refusal history?
ACUACULTURA AZTLAN (FEI: 3008101441) has 5 FDA import refusal record(s) in our database, spanning from 11/23/2010 to 11/23/2010.
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. ACUACULTURA AZTLAN's FEI number is 3008101441.
What types of violations has ACUACULTURA AZTLAN received?
ACUACULTURA AZTLAN 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 ACUACULTURA AZTLAN come from?
All FDA import refusal data for ACUACULTURA AZTLAN 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.