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Erik Suparjan

⚠️ Moderate Risk

FEI: 3011940020 • Pontianak, Kalimantan Barat • INDONESIA

FEI

FEI Number

3011940020

📍

Location

Pontianak, Kalimantan Barat

🇮🇩

Country

INDONESIA
🏢

Address

No., Jln. Kom Yos Sudarso; GG. SAPTAMARGA, Pontianak, Kalimantan Barat, Indonesia

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
5/23/2018
Latest Refusal
5/23/2018
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

24611×

UNSFDIETUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a dietary supplement or contain a dietary ingredient that renders it adulterated under section 402(a)(1) under the conditions of use recommended or suggested in the labeling of such dietary supplement.

Refusal History

DateProductViolationsDivision
5/23/2018
54KYR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2461UNSFDIETUS
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Erik Suparjan's FDA import refusal history?

Erik Suparjan (FEI: 3011940020) has 1 FDA import refusal record(s) in our database, spanning from 5/23/2018 to 5/23/2018.

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. Erik Suparjan's FEI number is 3011940020.

What types of violations has Erik Suparjan received?

Erik Suparjan 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 Erik Suparjan come from?

All FDA import refusal data for Erik Suparjan 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.