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EMIMAR, S.A.

Low Risk

FEI: 3012644031 • Santiago • DOMINICAN REPUBLIC

FEI

FEI Number

3012644031

📍

Location

Santiago

🇩🇴
🏢

Address

Las Palomas Licey Calle, , Santiago, , Dominican Republic

Low Risk

FDA Import Risk Assessment

22.8
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
8/26/2022
Latest Refusal
8/26/2022
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
32.4×20%
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

38601×

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.

Refusal History

DateProductViolationsDivision
8/26/2022
98DCA05ROLL-YOUR-OWN TOBACCO, LOOSE LEAF, LIGHT, MILD, OR LOW
3860TP USERFEE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

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

EMIMAR, S.A. (FEI: 3012644031) has 1 FDA import refusal record(s) in our database, spanning from 8/26/2022 to 8/26/2022.

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. EMIMAR, S.A.'s FEI number is 3012644031.

What types of violations has EMIMAR, S.A. received?

EMIMAR, S.A. 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 EMIMAR, S.A. come from?

All FDA import refusal data for EMIMAR, 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.