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Jose Sosa

⚠️ Moderate Risk

FEI: 3003881649 • Ladyville, Belize • BELIZE

FEI

FEI Number

3003881649

📍

Location

Ladyville, Belize

🇧🇿

Country

BELIZE
🏢

Address

13.5 Mile, , Ladyville, Belize, Belize

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
2/3/2003
Latest Refusal
2/3/2003
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

1794×

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
2/3/2003
65PCA02SILDENAFIL CITRATE (REGULATOR)
179AGR RX
New Orleans District Office (NOL-DO)
2/3/2003
65PCA02SILDENAFIL CITRATE (REGULATOR)
179AGR RX
New Orleans District Office (NOL-DO)
2/3/2003
65PCA02SILDENAFIL CITRATE (REGULATOR)
179AGR RX
New Orleans District Office (NOL-DO)
2/3/2003
65PCA02SILDENAFIL CITRATE (REGULATOR)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Jose Sosa's FDA import refusal history?

Jose Sosa (FEI: 3003881649) has 4 FDA import refusal record(s) in our database, spanning from 2/3/2003 to 2/3/2003.

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. Jose Sosa's FEI number is 3003881649.

What types of violations has Jose Sosa received?

Jose Sosa 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 Jose Sosa come from?

All FDA import refusal data for Jose Sosa 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.