HEIP LOI
⚠️ Moderate Risk
FEI: 3013932052 • Kien Giang • VIETNAM
FEI Number
3013932052
Location
Kien Giang
Country
VIETNAMAddress
97, Nguyen Hung Son, City, Kien Giang, , 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
MFRHACCP
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).
FILTH
The cosmetic appears to consist in whole or in part of any filthy, putrid, or decomposed substance.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/30/2017 | 16AYH23MULLET | Division of Southeast Imports (DSEI) | |
| 10/30/2017 | 16JGH05SHRIMP & PRAWNS | Division of Southeast Imports (DSEI) | |
| 10/30/2017 | 16MYY07CUTTLEFISH, OTHER AQUATIC SPECIES | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is HEIP LOI's FDA import refusal history?
HEIP LOI (FEI: 3013932052) has 3 FDA import refusal record(s) in our database, spanning from 10/30/2017 to 10/30/2017.
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. HEIP LOI's FEI number is 3013932052.
What types of violations has HEIP LOI received?
HEIP LOI 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 HEIP LOI come from?
All FDA import refusal data for HEIP LOI 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.