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EXOFRUT S.A.

⚠️ Moderate Risk

FEI: 3004381732 • Guayaquil • ECUADOR

FEI

FEI Number

3004381732

📍

Location

Guayaquil

🇪🇨

Country

ECUADOR
🏢

Address

Km 19.5 Via A La Costa, , Guayaquil, , Ecuador

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
2/22/2013
Latest Refusal
6/6/2012
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
2/22/2013
21VGD20STARFRUIT, CARAMBOLA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
241PESTICIDE
Seattle District Office (SEA-DO)
6/6/2012
21VGD20STARFRUIT, CARAMBOLA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
241PESTICIDE
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is EXOFRUT S.A.'s FDA import refusal history?

EXOFRUT S.A. (FEI: 3004381732) has 2 FDA import refusal record(s) in our database, spanning from 6/6/2012 to 2/22/2013.

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. EXOFRUT S.A.'s FEI number is 3004381732.

What types of violations has EXOFRUT S.A. received?

EXOFRUT S.A. 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 EXOFRUT S.A. come from?

All FDA import refusal data for EXOFRUT S.A. 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.