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Citrocorp S de PR de RL

⚠️ Moderate Risk

FEI: 3010012107 • Escuinapa, Sinaloa • MEXICO

FEI

FEI Number

3010012107

📍

Location

Escuinapa, Sinaloa

🇲🇽

Country

MEXICO
🏢

Address

Carretera Federal Libre Mexico-Nogales Km 1107, , Escuinapa, Sinaloa, Mexico

Moderate Risk

FDA Import Risk Assessment

47.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/29/2012
Latest Refusal
4/13/2010
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
11.8×10%
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
10/29/2012
21TFC99SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE, N.E.C.
9SALMONELLA
Southwest Import District Office (SWI-DO)
6/20/2011
21TFC99SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE, N.E.C.
9SALMONELLA
Southwest Import District Office (SWI-DO)
4/13/2010
23BGT05COCONUT, SHELLED
9SALMONELLA
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Citrocorp S de PR de RL's FDA import refusal history?

Citrocorp S de PR de RL (FEI: 3010012107) has 3 FDA import refusal record(s) in our database, spanning from 4/13/2010 to 10/29/2012.

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. Citrocorp S de PR de RL's FEI number is 3010012107.

What types of violations has Citrocorp S de PR de RL received?

Citrocorp S de PR de RL 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 Citrocorp S de PR de RL come from?

All FDA import refusal data for Citrocorp S de PR de RL 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.