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PT Sekar Mulia (Representative Office)

⚠️ Moderate Risk

FEI: 1000111888 • Jakarta Utara • INDONESIA

FEI

FEI Number

1000111888

📍

Location

Jakarta Utara

🇮🇩

Country

INDONESIA
🏢

Address

JL Muara Baru Ujung, , Jakarta Utara, , Indonesia

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/25/2002
Latest Refusal
10/25/2002
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

91×

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
10/25/2002
16XGD21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
9SALMONELLA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT Sekar Mulia (Representative Office)'s FDA import refusal history?

PT Sekar Mulia (Representative Office) (FEI: 1000111888) has 1 FDA import refusal record(s) in our database, spanning from 10/25/2002 to 10/25/2002.

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 Sekar Mulia (Representative Office)'s FEI number is 1000111888.

What types of violations has PT Sekar Mulia (Representative Office) received?

PT Sekar Mulia (Representative Office) 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 Sekar Mulia (Representative Office) come from?

All FDA import refusal data for PT Sekar Mulia (Representative Office) 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.