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Laboratorios Ameripharma S.A.

⚠️ Moderate Risk

FEI: 3003834627 • Santo Domingo De Guzman, Distrito Nacional • DOMINICAN REPUBLIC

FEI

FEI Number

3003834627

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Location

Santo Domingo De Guzman, Distrito Nacional

🇩🇴
🏢

Address

Zona Industrial de Haina, R.D., , Santo Domingo De Guzman, Distrito Nacional, Dominican Republic

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
1/23/2003
Latest Refusal
1/23/2003
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1791×

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
1/23/2003
64MCB01CLOMIPHENE CITRATE (GONAD-STIMULATING PRINCIPLE)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Laboratorios Ameripharma S.A.'s FDA import refusal history?

Laboratorios Ameripharma S.A. (FEI: 3003834627) has 1 FDA import refusal record(s) in our database, spanning from 1/23/2003 to 1/23/2003.

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. Laboratorios Ameripharma S.A.'s FEI number is 3003834627.

What types of violations has Laboratorios Ameripharma S.A. received?

Laboratorios Ameripharma S.A. 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 Laboratorios Ameripharma S.A. come from?

All FDA import refusal data for Laboratorios Ameripharma S.A. 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.