Brites Vaz & Irmaos
FDA import alert and refusal historyGafanha da Nazare, PortugalFEI 3009267925
As of October 26, 2026, Brites Vaz & Irmaos is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between January 3, 2019 and August 29, 2019, most often for seafood haccp requirements not met (MFRHACCP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cod · MFRHACCP
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Brites Vaz & Irmaos
8 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- MFRHACCP7 refused lines
Seafood HACCP requirements not met
The seafood appeared to have been processed without meeting the seafood HACCP requirements in 21 CFR 123.6(a) and 123.8(a), so it is treated as prepared under insanitary conditions.
Questions about Brites Vaz & Irmaos
- Is Brites Vaz & Irmaos on an FDA import alert?
- No listing for Brites Vaz & Irmaos appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
- Has FDA refused shipments from Brites Vaz & Irmaos?
- Yes. FDA refused 7 shipment lines from Brites Vaz & Irmaos between January 3, 2019 and August 29, 2019. The most recent, on August 29, 2019, was cod, charged as MFRHACCP (seafood haccp requirements not met).
- Why did FDA refuse Brites Vaz & Irmaos's shipments?
- The most frequent charge is MFRHACCP (seafood haccp requirements not met, 7 lines).
- When was Brites Vaz & Irmaos last inspected by FDA?
- FDA's most recent inspection of Brites Vaz & Irmaos with a final classification is dated February 18, 2014 and was classified OAI (Official Action Indicated).
- What is Brites Vaz & Irmaos's FEI number?
- Brites Vaz & Irmaos's FDA Establishment Identifier (FEI) is 3009267925.
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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.