Manh Ha Co
⚠️ Moderate Risk
FEI: 3005372321 • Fau City • VIETNAM
FEI Number
3005372321
Location
Fau City
Country
VIETNAMAddress
82 Le Loi Ward 4 Vung, , Fau 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
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/12/2005 | 16AGC42SWORDFISH | 251POISONOUS | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Manh Ha Co's FDA import refusal history?
Manh Ha Co (FEI: 3005372321) has 1 FDA import refusal record(s) in our database, spanning from 12/12/2005 to 12/12/2005.
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. Manh Ha Co's FEI number is 3005372321.
What types of violations has Manh Ha Co received?
Manh Ha Co 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 Manh Ha Co come from?
All FDA import refusal data for Manh Ha Co 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.