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Rsl Blunt Productions S.A.

⚠️ Moderate Risk

FEI: 3010297996 • Santiago • DOMINICAN REPUBLIC

FEI

FEI Number

3010297996

📍

Location

Santiago

🇩🇴
🏢

Address

Carretera Duarte Km 5, , Santiago, , Dominican Republic

Moderate Risk

FDA Import Risk Assessment

36.9
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
11/1/2022
Latest Refusal
11/1/2022
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
28.8×30%
Recency
36.2×20%
Frequency
50.0×10%
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

35205×

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.

38515×

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.

38525×

TPLACKSNC

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(B) of the FD&C Act in that the label does not provide an accurate statement of the quantity of contents in terms of weight, measure or numerical count.

38545×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

Refusal History

DateProductViolationsDivision
11/1/2022
98DCA01ROLL-YOUR-OWN TOBACCO, LOOSE LEAF
3520TP FLAVOR
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/1/2022
98DCA01ROLL-YOUR-OWN TOBACCO, LOOSE LEAF
3520TP FLAVOR
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/1/2022
98DCA01ROLL-YOUR-OWN TOBACCO, LOOSE LEAF
3520TP FLAVOR
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/1/2022
98DCA01ROLL-YOUR-OWN TOBACCO, LOOSE LEAF
3520TP FLAVOR
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/1/2022
98DCA01ROLL-YOUR-OWN TOBACCO, LOOSE LEAF
3520TP FLAVOR
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Rsl Blunt Productions S.A.'s FDA import refusal history?

Rsl Blunt Productions S.A. (FEI: 3010297996) has 5 FDA import refusal record(s) in our database, spanning from 11/1/2022 to 11/1/2022.

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. Rsl Blunt Productions S.A.'s FEI number is 3010297996.

What types of violations has Rsl Blunt Productions S.A. received?

Rsl Blunt Productions S.A. has been cited for 4 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 Rsl Blunt Productions S.A. come from?

All FDA import refusal data for Rsl Blunt Productions 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.