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Benito Mateos-Nevado Artero

⚠️ Moderate Risk

FEI: 3003444772 • Mairena Del Aljarafe, Sevilla • SPAIN

FEI

FEI Number

3003444772

📍

Location

Mairena Del Aljarafe, Sevilla

🇪🇸

Country

SPAIN
🏢

Address

Pinar De Simon Verde, , Mairena Del Aljarafe, Sevilla, Spain

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
1/6/2002
Latest Refusal
1/6/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1792×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
1/6/2002
66VCB99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
1/6/2002
66VCB99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Benito Mateos-Nevado Artero's FDA import refusal history?

Benito Mateos-Nevado Artero (FEI: 3003444772) has 2 FDA import refusal record(s) in our database, spanning from 1/6/2002 to 1/6/2002.

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. Benito Mateos-Nevado Artero's FEI number is 3003444772.

What types of violations has Benito Mateos-Nevado Artero received?

Benito Mateos-Nevado Artero 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 Benito Mateos-Nevado Artero come from?

All FDA import refusal data for Benito Mateos-Nevado Artero 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.