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Kleppe SA Plant 1

⚠️ Moderate Risk

FEI: 3009816170 • Cipolletti, Rio Negro • ARGENTINA

FEI

FEI Number

3009816170

📍

Location

Cipolletti, Rio Negro

🇦🇷

Country

ARGENTINA
🏢

Address

Calle Gral O Higgins 185, , Cipolletti, Rio Negro, Argentina

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/16/2007
Latest Refusal
5/16/2007
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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.

Refusal History

DateProductViolationsDivision
5/16/2007
20NFB01APPLE (CORE FRUIT)
249FILTHY
Philadelphia District Office (PHI-DO)
5/16/2007
20NFB03PEAR (CORE FRUIT)
249FILTHY
Philadelphia District Office (PHI-DO)
5/16/2007
20NFB01APPLE (CORE FRUIT)
249FILTHY
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Kleppe SA Plant 1's FDA import refusal history?

Kleppe SA Plant 1 (FEI: 3009816170) has 3 FDA import refusal record(s) in our database, spanning from 5/16/2007 to 5/16/2007.

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. Kleppe SA Plant 1's FEI number is 3009816170.

What types of violations has Kleppe SA Plant 1 received?

Kleppe SA Plant 1 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 Kleppe SA Plant 1 come from?

All FDA import refusal data for Kleppe SA Plant 1 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.