ImportRefusal LogoImportRefusal

PT Olam Indonesia

⚠️ Moderate Risk

FEI: 3004354160 • Bandarlampung, Lampung • INDONESIA

FEI

FEI Number

3004354160

📍

Location

Bandarlampung, Lampung

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Ki Agus Anang 36, , Bandarlampung, Lampung, Indonesia

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/14/2008
Latest Refusal
2/14/2008
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

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
2/14/2008
28BHT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)
2/14/2008
28BHT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)
2/14/2008
28BHT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)

Frequently Asked Questions

What is PT Olam Indonesia's FDA import refusal history?

PT Olam Indonesia (FEI: 3004354160) has 3 FDA import refusal record(s) in our database, spanning from 2/14/2008 to 2/14/2008.

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 Olam Indonesia's FEI number is 3004354160.

What types of violations has PT Olam Indonesia received?

PT Olam Indonesia 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 Olam Indonesia come from?

All FDA import refusal data for PT Olam Indonesia 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.