PT Anugerah Lestari Abadi
⚠️ Moderate Risk
FEI: 3011867543 • Bekasi, Jabotabek • INDONESIA
FEI Number
3011867543
Location
Bekasi, Jabotabek
Country
INDONESIAAddress
Jl raya Narogong Km 12 Pangkalan II No 4, , Bekasi, Jabotabek, 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.
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
Frequently Asked Questions
What is PT Anugerah Lestari Abadi's FDA import refusal history?
PT Anugerah Lestari Abadi (FEI: 3011867543) has 1 FDA import refusal record(s) in our database, spanning from 5/16/2017 to 5/16/2017.
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 Anugerah Lestari Abadi's FEI number is 3011867543.
What types of violations has PT Anugerah Lestari Abadi received?
PT Anugerah Lestari Abadi has been cited for 2 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 Anugerah Lestari Abadi come from?
All FDA import refusal data for PT Anugerah Lestari Abadi 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.