Vietrosco
⚠️ Moderate Risk
FEI: 3003215334 • Hochiminh City • VIETNAM
FEI Number
3003215334
Location
Hochiminh City
Country
VIETNAMAddress
14th Ward, 11th District, 26; 100, Binh Thoi St, Hochiminh City, , Vietnam
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.
VETDRUGRES
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/22/2013 | 16JGN01CRAB | 249FILTHY | New York District Office (NYK-DO) |
| 7/6/2009 | 16JGO01CRAB | 2860VETDRUGRES | Florida District Office (FLA-DO) |
| 3/2/2009 | 16AGD51MAHI MAHI | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 3/2/2009 | 16AGD37SNAPPER (RED, GRAY, MALABAR, ETC.) | 249FILTHY | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Vietrosco's FDA import refusal history?
Vietrosco (FEI: 3003215334) has 4 FDA import refusal record(s) in our database, spanning from 3/2/2009 to 3/22/2013.
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. Vietrosco's FEI number is 3003215334.
What types of violations has Vietrosco received?
Vietrosco 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 Vietrosco come from?
All FDA import refusal data for Vietrosco 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.