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Productos Negrini S.A.

⚠️ Moderate Risk

FEI: 3004254603 • La Valencia, Heredia • COSTA RICA

FEI

FEI Number

3004254603

📍

Location

La Valencia, Heredia

🇨🇷

Country

COSTA RICA
🏢

Address

Del Megasuper de la Valencia 200 metros, este y 200 metros norte, La Valencia, Heredia, Costa Rica

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

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

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

831×

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
2/12/2003
37JCT07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

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

Productos Negrini S.A. (FEI: 3004254603) has 1 FDA import refusal record(s) in our database, spanning from 2/12/2003 to 2/12/2003.

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 S.A.'s FEI number is 3004254603.

What types of violations has Productos Negrini S.A. received?

Productos Negrini 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 Productos Negrini S.A. come from?

All FDA import refusal data for Productos Negrini 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.