Dong Nai Livestock Company
⚠️ Moderate Risk
FEI: 3009788610 • Bien Hoa, VN-39 • VIETNAM
FEI Number
3009788610
Location
Bien Hoa, VN-39
Country
VIETNAMAddress
238 National Route, No1, Tan Hiep, Bien Hoa, VN-39, 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
PESTICIDE2
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/10/2014 | 25QEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 3721PESTICIDE2 | Baltimore District Office (BLT-DO) |
| 10/23/2014 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 10/20/2014 | 25SEE03MUSHROOM, STRAW, FUNGI PRODUCTS, N.E.C. | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 9/24/2014 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 3721PESTICIDE2 | Division of Southeast Imports (DSEI) |
| 9/24/2014 | 25QEE04MUSHROOM, SHIITAKE, PIECES AND STEMS, SLICED | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 9/23/2014 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
| 9/17/2014 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
| 8/13/2014 | 25PGT03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | New York District Office (NYK-DO) | |
| 5/14/2014 | 25QEE04MUSHROOM, SHIITAKE, PIECES AND STEMS, SLICED | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 10/20/2004 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 83NO PROCESS | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Dong Nai Livestock Company's FDA import refusal history?
Dong Nai Livestock Company (FEI: 3009788610) has 10 FDA import refusal record(s) in our database, spanning from 10/20/2004 to 11/10/2014.
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. Dong Nai Livestock Company's FEI number is 3009788610.
What types of violations has Dong Nai Livestock Company received?
Dong Nai Livestock Company 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 Dong Nai Livestock Company come from?
All FDA import refusal data for Dong Nai Livestock Company 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.