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PLATAFORMA ARCOIRIS, S. A.

⚠️ Moderate Risk

FEI: 3012657221 • SANTIAGO • DOMINICAN REPUBLIC

FEI

FEI Number

3012657221

📍

Location

SANTIAGO

🇩🇴
🏢

Address

Calle Santa Ana NO. 28, , Navarrete, SANTIAGO, , Dominican Republic

Moderate Risk

FDA Import Risk Assessment

45.4
LowModerateHighCritical

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

Statistics

15
Total Refusals
2
Unique Violations
7/18/2023
Latest Refusal
4/4/2022
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
44.6×30%
Recency
50.3×20%
Frequency
100.0×10%
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

386014×

TP USERFEE

This article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that the tobacco product appears to be adulterated under Section 902(4) because the importer of the tobacco product failed to pay a user fee assessed to such importer pursuant to Section 919 by the date specified in Section 919 or by the 30th day after final agency action on a resolution of any dispute as to the amount of the fee.

38511×

TPLACKFIRM

This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.

Refusal History

DateProductViolationsDivision
7/18/2023
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
5/12/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
5/4/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
5/4/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
5/4/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
5/4/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/26/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/26/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/14/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/11/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/11/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/8/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/8/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/8/2022
98GAA02CIGAR
3860TP USERFEE
Division of Southeast Imports (DSEI)
4/4/2022
98GAA02CIGAR
3851TPLACKFIRM
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PLATAFORMA ARCOIRIS, S. A.'s FDA import refusal history?

PLATAFORMA ARCOIRIS, S. A. (FEI: 3012657221) has 15 FDA import refusal record(s) in our database, spanning from 4/4/2022 to 7/18/2023.

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. PLATAFORMA ARCOIRIS, S. A.'s FEI number is 3012657221.

What types of violations has PLATAFORMA ARCOIRIS, S. A. received?

PLATAFORMA ARCOIRIS, S. A. 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 PLATAFORMA ARCOIRIS, S. A. come from?

All FDA import refusal data for PLATAFORMA ARCOIRIS, S. A. 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.