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Nefis Srl

⚠️ Moderate Risk

FEI: 3010135881 • Cojusna, Straseni • MOLDOVA

FEI

FEI Number

3010135881

📍

Location

Cojusna, Straseni

🇲🇩

Country

MOLDOVA
🏢

Address

Str. Rivaz Lomtadze 2/3, R-Ul Straseni, , Cojusna, Straseni, Moldova

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
7/24/2013
Latest Refusal
7/24/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

114×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
7/24/2013
33CFT02CARAMEL CANDY PIECES, HARD, WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
7/24/2013
33EFT02CARAMEL CANDY PIECES, HARD, WITHOUT NUTS OR FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
7/24/2013
33EFT02CARAMEL CANDY PIECES, HARD, WITHOUT NUTS OR FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
7/24/2013
03RFT60WAFFLES WITHOUT CUSTARD OR CREAM FILLING
11UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Nefis Srl's FDA import refusal history?

Nefis Srl (FEI: 3010135881) has 4 FDA import refusal record(s) in our database, spanning from 7/24/2013 to 7/24/2013.

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. Nefis Srl's FEI number is 3010135881.

What types of violations has Nefis Srl received?

Nefis Srl 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 Nefis Srl come from?

All FDA import refusal data for Nefis Srl 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.