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PT Gorom Kencana

⚠️ Moderate Risk

FEI: 3009572441 • Surabaya, Jawa Timur • INDONESIA

FEI

FEI Number

3009572441

📍

Location

Surabaya, Jawa Timur

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Tanjung Sari No. 1, Mas, Surabaya, Jawa Timur, Indonesia

Moderate Risk

FDA Import Risk Assessment

47.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/8/2010
Latest Refusal
9/10/2007
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
12.4×10%
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

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
2/8/2010
28BGT30NUTMEG, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)
2/5/2010
28BGT30NUTMEG, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)
9/10/2007
28BGT30NUTMEG, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)

Frequently Asked Questions

What is PT Gorom Kencana's FDA import refusal history?

PT Gorom Kencana (FEI: 3009572441) has 3 FDA import refusal record(s) in our database, spanning from 9/10/2007 to 2/8/2010.

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 Gorom Kencana's FEI number is 3009572441.

What types of violations has PT Gorom Kencana received?

PT Gorom Kencana 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 Gorom Kencana come from?

All FDA import refusal data for PT Gorom Kencana 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.