Kien Giang Sea Product Corporation
✅ Low Risk
FEI: 3009946680 • Rach Gia, Kien Giang • VIETNAM
FEI Number
3009946680
Location
Rach Gia, Kien Giang
Country
VIETNAMAddress
62, Ngo Thoi Nhiem Street, An Binh Ward, , Rach Gia, Kien Giang, Vietnam
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/23/2005 | 16YGD03FISH PASTE, FISHERY PRODUCTS, N.E.C. | 218LIST INGRE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Kien Giang Sea Product Corporation's FDA import refusal history?
Kien Giang Sea Product Corporation (FEI: 3009946680) has 1 FDA import refusal record(s) in our database, spanning from 2/23/2005 to 2/23/2005.
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. Kien Giang Sea Product Corporation's FEI number is 3009946680.
What types of violations has Kien Giang Sea Product Corporation received?
Kien Giang Sea Product Corporation 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 Kien Giang Sea Product Corporation come from?
All FDA import refusal data for Kien Giang Sea Product Corporation 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.