Pt. Gabungan Era Mandiri
⚠️ Moderate Risk
FEI: 3003374825 • Jakarta Indonesia • INDONESIA
FEI Number
3003374825
Location
Jakarta Indonesia
Country
INDONESIAAddress
Pelabuhan Perikanan Jl, , Jakarta Indonesia, , Indonesia
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
Frequently Asked Questions
What is Pt. Gabungan Era Mandiri's FDA import refusal history?
Pt. Gabungan Era Mandiri (FEI: 3003374825) has 2 FDA import refusal record(s) in our database, spanning from 7/29/2002 to 6/5/2008.
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. Gabungan Era Mandiri's FEI number is 3003374825.
What types of violations has Pt. Gabungan Era Mandiri received?
Pt. Gabungan Era Mandiri 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. Gabungan Era Mandiri come from?
All FDA import refusal data for Pt. Gabungan Era Mandiri 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.