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Exp. Proyimar S.A

⚠️ Moderate Risk

FEI: 3008856098 • Guayaquil, Guayas • ECUADOR

FEI

FEI Number

3008856098

📍

Location

Guayaquil, Guayas

🇪🇨

Country

ECUADOR
🏢

Address

Km 8 1/2 Via Duale, , Guayaquil, Guayas, Ecuador

Moderate Risk

FDA Import Risk Assessment

36.6
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
11/10/2021
Latest Refusal
11/10/2021
Earliest Refusal

Score Breakdown

Violation Severity
61.3×40%
Refusal Volume
25.9×30%
Recency
1.8×20%
Frequency
40.0×10%
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

2493×

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.

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2531×

STD IDENT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
11/10/2021
16JGD01CRAB
253STD IDENT
320LACKS FIRM
Division of Northeast Imports (DNEI)
11/10/2021
16EGD02CLAMS
249FILTHY
473LABELING
Division of Northeast Imports (DNEI)
11/10/2021
16EGD02CLAMS
249FILTHY
473LABELING
Division of Northeast Imports (DNEI)
11/10/2021
16EGD02CLAMS
249FILTHY
473LABELING
Division of Northeast Imports (DNEI)

Frequently Asked Questions

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

Exp. Proyimar S.A (FEI: 3008856098) has 4 FDA import refusal record(s) in our database, spanning from 11/10/2021 to 11/10/2021.

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. Exp. Proyimar S.A's FEI number is 3008856098.

What types of violations has Exp. Proyimar S.A received?

Exp. Proyimar S.A has been cited for 4 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 Exp. Proyimar S.A come from?

All FDA import refusal data for Exp. Proyimar 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.