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IBERPAPEL, S.L.

⚠️ Moderate Risk

FEI: 3012568145 • Alicante • SPAIN

FEI

FEI Number

3012568145

📍

Location

Alicante

🇪🇸

Country

SPAIN
🏢

Address

Benimarfull, Pol. Ind. La Creueta, S, Alicante, , Spain

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/19/2022
Latest Refusal
12/19/2022
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
24.7×20%
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

35201×

TP FLAVOR

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.

Refusal History

DateProductViolationsDivision
12/19/2022
98FCA01ROLL-YOUR-OWN PAPER
3520TP FLAVOR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is IBERPAPEL, S.L.'s FDA import refusal history?

IBERPAPEL, S.L. (FEI: 3012568145) has 1 FDA import refusal record(s) in our database, spanning from 12/19/2022 to 12/19/2022.

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. IBERPAPEL, S.L.'s FEI number is 3012568145.

What types of violations has IBERPAPEL, S.L. received?

IBERPAPEL, S.L. 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 IBERPAPEL, S.L. come from?

All FDA import refusal data for IBERPAPEL, S.L. 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.