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Indapex

✅ Low Risk

FEI: 3003469983 • Nueva San Salvador, La Libertad • EL SALVADOR

FEI

FEI Number

3003469983

📍

Location

Nueva San Salvador, La Libertad

🇸🇻
🏢

Address

Residencial Bethania, , Nueva San Salvador, La Libertad, El Salvador

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
2
Unique Violations
5/23/2002
Latest Refusal
4/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

3281×

USUAL NAME

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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
5/23/2002
23KGT01PUMPKIN SEED (EDIBLE SEED)
328USUAL NAME
Los Angeles District Office (LOS-DO)
4/3/2002
02BGT01CORN, BOLTED MEAL OR FLOUR
473LABELING
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Indapex's FDA import refusal history?

Indapex (FEI: 3003469983) has 2 FDA import refusal record(s) in our database, spanning from 4/3/2002 to 5/23/2002.

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. Indapex's FEI number is 3003469983.

What types of violations has Indapex received?

Indapex has been cited for 2 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 Indapex come from?

All FDA import refusal data for Indapex 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.