G.F.I. Enterprises, Inc.
⚠️ High Risk
FEI: 3004270161 • Valenzuela, Metro Manila • PHILIPPINES
FEI Number
3004270161
Location
Valenzuela, Metro Manila
Country
PHILIPPINESAddress
63 J. P. Rizal Street, , Valenzuela, Metro Manila, Philippines
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
MYCOTOXIN
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous and deleterious substance, namely a mycotoxin (aflatoxin, deoxynivalenol, fumonisin, or ochratoxin A), which may render it injurious to health. Bears or contains:
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
HEALTH C
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/24/2022 | 23BGT07PEANUT, SHELLED | 3897MYCOTOXIN | Division of Northeast Imports (DNEI) |
| 10/13/2021 | 23BGT07PEANUT, SHELLED | 3897MYCOTOXIN | Division of West Coast Imports (DWCI) |
| 7/3/2019 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 7/3/2019 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 4/19/2019 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 4/11/2019 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 4/11/2019 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 2/14/2019 | 23BGE07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 12/11/2018 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Division of West Coast Imports (DWCI) |
| 8/29/2013 | 23BGT07PEANUT, SHELLED | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is G.F.I. Enterprises, Inc.'s FDA import refusal history?
G.F.I. Enterprises, Inc. (FEI: 3004270161) has 10 FDA import refusal record(s) in our database, spanning from 8/29/2013 to 1/24/2022.
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. G.F.I. Enterprises, Inc.'s FEI number is 3004270161.
What types of violations has G.F.I. Enterprises, Inc. received?
G.F.I. Enterprises, Inc. has been cited for 5 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 G.F.I. Enterprises, Inc. come from?
All FDA import refusal data for G.F.I. Enterprises, Inc. 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.