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LULJAN SULOVARI

⚠️ Moderate Risk

FEI: 3017833533 • Granarolo Dell'Emilia, Bologna • ITALY

FEI

FEI Number

3017833533

📍

Location

Granarolo Dell'Emilia, Bologna

🇮🇹

Country

ITALY
🏢

Address

Via Lionello Bettini 5, , Granarolo Dell'Emilia, Bologna, Italy

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/1/2021
Latest Refusal
2/1/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
2/1/2021
62UDA99ANTI-TUSSIVE/COLD N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LULJAN SULOVARI's FDA import refusal history?

LULJAN SULOVARI (FEI: 3017833533) has 1 FDA import refusal record(s) in our database, spanning from 2/1/2021 to 2/1/2021.

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. LULJAN SULOVARI's FEI number is 3017833533.

What types of violations has LULJAN SULOVARI received?

LULJAN SULOVARI 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 LULJAN SULOVARI come from?

All FDA import refusal data for LULJAN SULOVARI 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.