Barro Fiesta Manufacturing Inc
⚠️ Moderate Risk
FEI: 3001032722 • Pasig City • PHILIPPINES
FEI Number
3001032722
Location
Pasig City
Country
PHILIPPINESAddress
120 Alfonso, , Pasig City, , 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
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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).
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
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.
BACTERIA
The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/31/2008 | 16YCT12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C. | Florida District Office (FLA-DO) | |
| 5/14/2005 | 65RAL18SODIUM BICARBONATE (REPLENISHER) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 4/21/2005 | 24FCT08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 2/23/2005 | 16ACE01ANCHOVY | Los Angeles District Office (LOS-DO) | |
| 8/15/2002 | 16YCN12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C. | 306INSANITARY | Los Angeles District Office (LOS-DO) |
| 8/15/2002 | 16YCN12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C. | 306INSANITARY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Barro Fiesta Manufacturing Inc's FDA import refusal history?
Barro Fiesta Manufacturing Inc (FEI: 3001032722) has 6 FDA import refusal record(s) in our database, spanning from 8/15/2002 to 7/31/2008.
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. Barro Fiesta Manufacturing Inc's FEI number is 3001032722.
What types of violations has Barro Fiesta Manufacturing Inc received?
Barro Fiesta Manufacturing Inc has been cited for 6 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 Barro Fiesta Manufacturing Inc come from?
All FDA import refusal data for Barro Fiesta Manufacturing 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.