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Productos Negrini Ltda

⚠️ Moderate Risk

FEI: 3003787363 • Costa Rica • COSTA RICA

FEI

FEI Number

3003787363

📍

Location

Costa Rica

🇨🇷

Country

COSTA RICA
🏢

Address

Zona Industrial La, , Valencia,Costa Rica, , Costa Rica

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
11/12/2003
Latest Refusal
11/4/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
19.6×10%
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

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
11/12/2003
24KCI07PEPPER, SWEET, WITH SAUCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
11/4/2002
24KCI08PEPPER, HOT, WITH SAUCE
83NO PROCESS
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Productos Negrini Ltda's FDA import refusal history?

Productos Negrini Ltda (FEI: 3003787363) has 2 FDA import refusal record(s) in our database, spanning from 11/4/2002 to 11/12/2003.

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. Productos Negrini Ltda's FEI number is 3003787363.

What types of violations has Productos Negrini Ltda received?

Productos Negrini Ltda 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 Productos Negrini Ltda come from?

All FDA import refusal data for Productos Negrini Ltda 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.