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Fresomar Inc.

⚠️ High Risk

FEI: 3003548524 • Geneal Santos City • PHILIPPINES

FEI

FEI Number

3003548524

📍

Location

Geneal Santos City

🇵🇭
🏢

Address

9500 Dole Compound Calumpang, , Geneal Santos City, , Philippines

High Risk

FDA Import Risk Assessment

53.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

5
Total Refusals
1
Unique Violations
1/11/2005
Latest Refusal
1/11/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

2495×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
1/11/2005
16AGT51MAHI MAHI
249FILTHY
Los Angeles District Office (LOS-DO)
1/11/2005
16AGT51MAHI MAHI
249FILTHY
Los Angeles District Office (LOS-DO)
1/11/2005
16AGT51MAHI MAHI
249FILTHY
Los Angeles District Office (LOS-DO)
1/11/2005
16AGT51MAHI MAHI
249FILTHY
Los Angeles District Office (LOS-DO)
1/11/2005
16AGT51MAHI MAHI
249FILTHY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Fresomar Inc.'s FDA import refusal history?

Fresomar Inc. (FEI: 3003548524) has 5 FDA import refusal record(s) in our database, spanning from 1/11/2005 to 1/11/2005.

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. Fresomar Inc.'s FEI number is 3003548524.

What types of violations has Fresomar Inc. received?

Fresomar Inc. 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 Fresomar Inc. come from?

All FDA import refusal data for Fresomar Inc. 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.