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Dr Arturo Perez Ramirez

⚠️ Moderate Risk

FEI: 3005869435 • Ecatepec de Morelos, Mexico • MEXICO

FEI

FEI Number

3005869435

📍

Location

Ecatepec de Morelos, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Avenida Revolucion 63, Fracc. HOGARES MARLA, Ecatepec de Morelos, Mexico, Mexico

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
2
Unique Violations
9/13/2006
Latest Refusal
9/13/2006
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

Refusal History

DateProductViolationsDivision
9/13/2006
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
483DRUG NAME
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dr Arturo Perez Ramirez's FDA import refusal history?

Dr Arturo Perez Ramirez (FEI: 3005869435) has 1 FDA import refusal record(s) in our database, spanning from 9/13/2006 to 9/13/2006.

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. Dr Arturo Perez Ramirez's FEI number is 3005869435.

What types of violations has Dr Arturo Perez Ramirez received?

Dr Arturo Perez Ramirez has been cited for 2 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 Dr Arturo Perez Ramirez come from?

All FDA import refusal data for Dr Arturo Perez Ramirez 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.