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Neptuno S.A.

⚠️ High Risk

FEI: 1000592004 • Managua • NICARAGUA

FEI

FEI Number

1000592004

📍

Location

Managua

🇳🇮

Country

NICARAGUA
🏢

Address

Km 18 Carretera Nueva a Leon, , Managua, , Nicaragua

High Risk

FDA Import Risk Assessment

52.7
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

4
Total Refusals
1
Unique Violations
12/6/2022
Latest Refusal
5/26/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
23.4×20%
Frequency
2.3×10%
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

2494×

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.

Refusal History

DateProductViolationsDivision
12/6/2022
16AGT37SNAPPER (RED, GRAY, MALABAR, ETC.)
249FILTHY
Division of Southeast Imports (DSEI)
7/2/2013
16JGD06SPINY LOBSTER, ROCK LOBSTER
249FILTHY
Florida District Office (FLA-DO)
7/2/2013
16JGD06SPINY LOBSTER, ROCK LOBSTER
249FILTHY
Florida District Office (FLA-DO)
5/26/2005
16JGT05SHRIMP & PRAWNS
249FILTHY
Florida District Office (FLA-DO)

Frequently Asked Questions

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

Neptuno S.A. (FEI: 1000592004) has 4 FDA import refusal record(s) in our database, spanning from 5/26/2005 to 12/6/2022.

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. Neptuno S.A.'s FEI number is 1000592004.

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

Neptuno 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 Neptuno S.A. come from?

All FDA import refusal data for Neptuno 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.