ImportRefusal LogoImportRefusal

PT GIKEN PRECISION INDONESIA

⚠️ High Risk

FEI: 3009865005 • Batam, Riau • INDONESIA

FEI

FEI Number

3009865005

📍

Location

Batam, Riau

🇮🇩

Country

INDONESIA
🏢

Address

Jl. Yos Sudarso Citra Buana Industrial Park Ii Lot 2 Batu Ampar, , Batam, Riau, Indonesia

High Risk

FDA Import Risk Assessment

51.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
10/8/2025
Latest Refusal
10/8/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
94.7×20%
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

38421×

TP NO PMTA

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.

Refusal History

DateProductViolationsDivision
10/8/2025
98MEA03ENDS ATOMIZER
3842TP NO PMTA
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is PT GIKEN PRECISION INDONESIA's FDA import refusal history?

PT GIKEN PRECISION INDONESIA (FEI: 3009865005) has 1 FDA import refusal record(s) in our database, spanning from 10/8/2025 to 10/8/2025.

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 GIKEN PRECISION INDONESIA's FEI number is 3009865005.

What types of violations has PT GIKEN PRECISION INDONESIA received?

PT GIKEN PRECISION 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 GIKEN PRECISION INDONESIA come from?

All FDA import refusal data for PT GIKEN PRECISION 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.