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Mardianto

⚠️ Moderate Risk

FEI: 3011712223 • Pontianak • INDONESIA

FEI

FEI Number

3011712223

📍

Location

Pontianak

🇮🇩

Country

INDONESIA
🏢

Address

Jl Sei Raya Dalam Komp Kartika, , Pontianak, , Indonesia

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/13/2015
Latest Refusal
10/13/2015
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

21203×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

Refusal History

DateProductViolationsDivision
10/13/2015
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
10/13/2015
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
10/13/2015
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Mardianto's FDA import refusal history?

Mardianto (FEI: 3011712223) has 3 FDA import refusal record(s) in our database, spanning from 10/13/2015 to 10/13/2015.

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. Mardianto's FEI number is 3011712223.

What types of violations has Mardianto received?

Mardianto 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 Mardianto come from?

All FDA import refusal data for Mardianto 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.