PT. Anugrah Laut Indonesia
🚨 Critical Risk
FEI: 3020093558 • Tuban, Jawa Timur • INDONESIA
FEI Number
3020093558
Location
Tuban, Jawa Timur
Country
INDONESIAAddress
Jl. Rembang Tuban Km 40, Desa Bancar, Kecamatan Bancar, , Tuban, Jawa Timur, Indonesia
Critical Risk
FDA Import Risk Assessment
This firm has an extensive history of FDA import refusals with severe violations.
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.
HISTAMINE
The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2025 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 2360HISTAMINE | Division of West Coast Imports (DWCI) |
| 1/6/2025 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 2360HISTAMINE | Division of West Coast Imports (DWCI) |
| 1/6/2025 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 2360HISTAMINE | Division of West Coast Imports (DWCI) |
| 1/6/2025 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 2360HISTAMINE | Division of West Coast Imports (DWCI) |
| 1/6/2025 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 2360HISTAMINE | Division of West Coast Imports (DWCI) |
| 4/11/2024 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/11/2024 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/11/2024 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 12/28/2023 | 16JGD05SHRIMP & PRAWNS | Division of Northeast Imports (DNEI) | |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 6/15/2023 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is PT. Anugrah Laut Indonesia's FDA import refusal history?
PT. Anugrah Laut Indonesia (FEI: 3020093558) has 18 FDA import refusal record(s) in our database, spanning from 6/15/2023 to 1/6/2025.
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. Anugrah Laut Indonesia's FEI number is 3020093558.
What types of violations has PT. Anugrah Laut Indonesia received?
PT. Anugrah Laut Indonesia has been cited for 3 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. Anugrah Laut Indonesia come from?
All FDA import refusal data for PT. Anugrah Laut 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.