Barrio Fiesta Manufacturing Corporation
FDA import alert and refusal historyBulacan, PhilippinesFEI 3010106066
As of October 26, 2026, Barrio Fiesta Manufacturing Corporation is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 13, 2022, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Shrimp paste, fishery products, n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Barrio Fiesta Manufacturing Corporation
3 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2022
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Barrio Fiesta Manufacturing Corporation
- Is Barrio Fiesta Manufacturing Corporation on an FDA import alert?
- No listing for Barrio Fiesta Manufacturing Corporation appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Philippines page.
- Has FDA refused shipments from Barrio Fiesta Manufacturing Corporation?
- Yes. FDA refused 2 shipment lines from Barrio Fiesta Manufacturing Corporation on December 13, 2022. The most recent, on December 13, 2022, was shrimp paste, fishery products, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Barrio Fiesta Manufacturing Corporation's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- When was Barrio Fiesta Manufacturing Corporation last inspected by FDA?
- FDA's most recent inspection of Barrio Fiesta Manufacturing Corporation with a final classification is dated March 1, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Barrio Fiesta Manufacturing Corporation's FEI number?
- Barrio Fiesta Manufacturing Corporation's FDA Establishment Identifier (FEI) is 3010106066.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.