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Tri Suherdi

⚠️ Moderate Risk

FEI: 3011711454 • Kalimantan Bara • INDONESIA

FEI

FEI Number

3011711454

📍

Location

Kalimantan Bara

🇮🇩

Country

INDONESIA
🏢

Address

Dusun Tumuk Sambas, , Kalimantan Bara, , 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
10/26/2015
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
53PH99OTHER COSMETIC RAW MATERIALS, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
10/26/2015
53PH99OTHER COSMETIC RAW MATERIALS, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Tri Suherdi's FDA import refusal history?

Tri Suherdi (FEI: 3011711454) has 3 FDA import refusal record(s) in our database, spanning from 10/26/2015 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. Tri Suherdi's FEI number is 3011711454.

What types of violations has Tri Suherdi received?

Tri Suherdi 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 Tri Suherdi come from?

All FDA import refusal data for Tri Suherdi 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.