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M. Ridho Rizki Maulufi Alk

⚠️ Moderate Risk

FEI: 3011504962 • Pontianak • INDONESIA

FEI

FEI Number

3011504962

📍

Location

Pontianak

🇮🇩

Country

INDONESIA
🏢

Address

11 Jalan Tabrani Achmad Kimplex Gbk D, , 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
10/26/2015
Latest Refusal
10/16/2015
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
10/26/2015
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
10/26/2015
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
10/16/2015
53PH99OTHER COSMETIC RAW MATERIALS, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is M. Ridho Rizki Maulufi Alk's FDA import refusal history?

M. Ridho Rizki Maulufi Alk (FEI: 3011504962) has 3 FDA import refusal record(s) in our database, spanning from 10/16/2015 to 10/26/2015.

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. M. Ridho Rizki Maulufi Alk's FEI number is 3011504962.

What types of violations has M. Ridho Rizki Maulufi Alk received?

M. Ridho Rizki Maulufi Alk 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 M. Ridho Rizki Maulufi Alk come from?

All FDA import refusal data for M. Ridho Rizki Maulufi Alk 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.