Guzent
⚠️ Moderate Risk
FEI: 1000205535 • Quezon City, National Capital Region • PHILIPPINES
FEI Number
1000205535
Location
Quezon City, National Capital Region
Country
PHILIPPINESAddress
1237 Epifanio Delos Santos Avenue, , Quezon City, National Capital Region, Philippines
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
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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:
NUTRIT LBL
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 fails to bear the required nutrition information.
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.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
PESTICIDES
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:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/31/2016 | 24TGT99LEAF & STEM VEGETABLES, N.E.C. | 241PESTICIDE | Chicago District Office (CHI-DO) |
| 9/24/2014 | 21SGD02BANANA (SUBTROPICAL AND TROPICAL FRUIT) | 9SALMONELLA | Chicago District Office (CHI-DO) |
| 4/8/2014 | 24TGT99LEAF & STEM VEGETABLES, N.E.C. | 3721PESTICIDE2 | Chicago District Office (CHI-DO) |
| 1/10/2008 | 21SGD14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | 249FILTHY | Chicago District Office (CHI-DO) |
| 7/14/2006 | 28AGD99WHOLE SPICE, N.E.C. | 2920PESTICIDES | Chicago District Office (CHI-DO) |
| 2/6/2006 | 24AGI06GARBANZO BEAN | 62NEEDS FCE | Chicago District Office (CHI-DO) |
| 9/13/2002 | 24ACE06GARBANZO BEAN | Chicago District Office (CHI-DO) | |
| 7/31/2002 | 16YCP09FISH SAUCE, FISHERY PRODUCTS, N.E.C. | 249FILTHY | Chicago District Office (CHI-DO) |
| 4/12/2002 | 24AEE99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Guzent's FDA import refusal history?
Guzent (FEI: 1000205535) has 9 FDA import refusal record(s) in our database, spanning from 4/12/2002 to 5/31/2016.
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. Guzent's FEI number is 1000205535.
What types of violations has Guzent received?
Guzent has been cited for 8 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 Guzent come from?
All FDA import refusal data for Guzent 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.