ImportRefusal LogoImportRefusal

Pt. Trisila Utama Anugrah

⚠️ Moderate Risk

FEI: 1000350096 • Jakarta • INDONESIA

FEI

FEI Number

1000350096

📍

Location

Jakarta

🇮🇩

Country

INDONESIA
🏢

Address

Jin. Kayu Putih Utara C/17, , Jakarta, , Indonesia

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/5/2006
Latest Refusal
9/5/2006
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2492×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
9/5/2006
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Los Angeles District Office (LOS-DO)
9/5/2006
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Pt. Trisila Utama Anugrah's FDA import refusal history?

Pt. Trisila Utama Anugrah (FEI: 1000350096) has 2 FDA import refusal record(s) in our database, spanning from 9/5/2006 to 9/5/2006.

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. Pt. Trisila Utama Anugrah's FEI number is 1000350096.

What types of violations has Pt. Trisila Utama Anugrah received?

Pt. Trisila Utama Anugrah 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 Pt. Trisila Utama Anugrah come from?

All FDA import refusal data for Pt. Trisila Utama Anugrah 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.