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Agustin Ocumares

⚠️ Moderate Risk

FEI: 3004183112 • San Martin • DOMINICAN REPUBLIC

FEI

FEI Number

3004183112

📍

Location

San Martin

🇩🇴
🏢

Address

Edif Santanita Primer Piso, , San Martin, , Dominican Republic

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/31/2003
Latest Refusal
12/31/2003
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
12/31/2003
63XOY99DIAGOSTIC AID (DRUGS) N.E.C.
72NEW VET DR
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Agustin Ocumares's FDA import refusal history?

Agustin Ocumares (FEI: 3004183112) has 1 FDA import refusal record(s) in our database, spanning from 12/31/2003 to 12/31/2003.

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. Agustin Ocumares's FEI number is 3004183112.

What types of violations has Agustin Ocumares received?

Agustin Ocumares 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 Agustin Ocumares come from?

All FDA import refusal data for Agustin Ocumares 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.