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Ixtlahuacan, S.P.R. De R.L.

⚠️ Moderate Risk

FEI: 3002893999 • Colima • MEXICO

FEI

FEI Number

3002893999

📍

Location

Colima

🇲🇽

Country

MEXICO
🏢

Address

%, , Colima, , Mexico

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/23/2005
Latest Refusal
2/24/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
3/23/2005
22AFC01CANTALOUPE (VINE FRUIT)
9SALMONELLA
Southwest Import District Office (SWI-DO)
3/23/2005
22AFC01CANTALOUPE (VINE FRUIT)
9SALMONELLA
Southwest Import District Office (SWI-DO)
2/24/2005
22AFC01CANTALOUPE (VINE FRUIT)
9SALMONELLA
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Ixtlahuacan, S.P.R. De R.L.'s FDA import refusal history?

Ixtlahuacan, S.P.R. De R.L. (FEI: 3002893999) has 3 FDA import refusal record(s) in our database, spanning from 2/24/2005 to 3/23/2005.

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. Ixtlahuacan, S.P.R. De R.L.'s FEI number is 3002893999.

What types of violations has Ixtlahuacan, S.P.R. De R.L. received?

Ixtlahuacan, S.P.R. De R.L. 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 Ixtlahuacan, S.P.R. De R.L. come from?

All FDA import refusal data for Ixtlahuacan, S.P.R. De R.L. 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.