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COREX

⚠️ Moderate Risk

FEI: 3008260006 • Battipaglia, Salerno • ITALY

FEI

FEI Number

3008260006

📍

Location

Battipaglia, Salerno

🇮🇹

Country

ITALY
🏢

Address

Zona Industriale Snc, , Battipaglia, Salerno, Italy

Moderate Risk

FDA Import Risk Assessment

29.2
LowModerateHighCritical

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

Statistics

6
Total Refusals
2
Unique Violations
3/23/2020
Latest Refusal
7/31/2008
Earliest Refusal

Score Breakdown

Violation Severity
48.3×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
5.2×10%
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

2535×

STD IDENT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.

111×

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
3/23/2020
04AGT99MACARONI AND SPAGHETTI PRODUCTS,N.E.C.
253STD IDENT
Division of West Coast Imports (DWCI)
3/22/2016
04AGT05SPAGHETTI
253STD IDENT
Los Angeles District Office (LOS-DO)
2/19/2016
04AGT05SPAGHETTI
253STD IDENT
New York District Office (NYK-DO)
12/30/2015
04AGT05SPAGHETTI
253STD IDENT
Division of West Coast Imports (DWCI)
11/2/2015
04AGT05SPAGHETTI
253STD IDENT
Los Angeles District Office (LOS-DO)
7/31/2008
04AHT01MACARONI ENRICHED
11UNSAFE COL
New York District Office (NYK-DO)

Frequently Asked Questions

What is COREX's FDA import refusal history?

COREX (FEI: 3008260006) has 6 FDA import refusal record(s) in our database, spanning from 7/31/2008 to 3/23/2020.

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. COREX's FEI number is 3008260006.

What types of violations has COREX received?

COREX has been cited for 2 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 COREX come from?

All FDA import refusal data for COREX 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.