Aurora Pouch Products Industry Co, Ltd.
⚠️ Moderate Risk
FEI: 3000197834 • Samutsakorn • THAILAND
FEI Number
3000197834
Location
Samutsakorn
Country
THAILANDAddress
Thacheen, Amphur Muang, 33 Moo 6 Thonburi-Paktom Rd, Samutsakorn, , Thailand
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/17/2007 | 16AGE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Florida District Office (FLA-DO) |
| 3/21/2005 | 16ADE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Seattle District Office (SEA-DO) |
| 3/21/2005 | 16ADE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Aurora Pouch Products Industry Co, Ltd.'s FDA import refusal history?
Aurora Pouch Products Industry Co, Ltd. (FEI: 3000197834) has 3 FDA import refusal record(s) in our database, spanning from 3/21/2005 to 8/17/2007.
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. Aurora Pouch Products Industry Co, Ltd.'s FEI number is 3000197834.
What types of violations has Aurora Pouch Products Industry Co, Ltd. received?
Aurora Pouch Products Industry Co, Ltd. 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 Aurora Pouch Products Industry Co, Ltd. come from?
All FDA import refusal data for Aurora Pouch Products Industry Co, Ltd. 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.