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PT. SHIKAMASE LAKASANA CIPTA

⚠️ Moderate Risk

FEI: 3012065950 • Bekasi • INDONESIA

FEI

FEI Number

3012065950

📍

Location

Bekasi

🇮🇩

Country

INDONESIA
🏢

Address

Jl. raya Kalimalang No., , Bekasi, , 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
12/29/2017
Latest Refusal
12/29/2017
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

2493×

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
12/29/2017
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Division of Northeast Imports (DNEI)
12/29/2017
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Division of Northeast Imports (DNEI)
12/29/2017
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is PT. SHIKAMASE LAKASANA CIPTA's FDA import refusal history?

PT. SHIKAMASE LAKASANA CIPTA (FEI: 3012065950) has 3 FDA import refusal record(s) in our database, spanning from 12/29/2017 to 12/29/2017.

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. SHIKAMASE LAKASANA CIPTA's FEI number is 3012065950.

What types of violations has PT. SHIKAMASE LAKASANA CIPTA received?

PT. SHIKAMASE LAKASANA CIPTA 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. SHIKAMASE LAKASANA CIPTA come from?

All FDA import refusal data for PT. SHIKAMASE LAKASANA CIPTA 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.