Brunel

1 record, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• NEEDS FCE1 refused line

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Brunel

Is Brunel on an FDA import alert?

No listing for Brunel appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.

Has FDA refused shipments from Brunel?

Yes. FDA refused 1 shipment line from Brunel on July 1, 2025. The most recent, on July 1, 2025, was vegetable & vegetable products not mentioned elsewhere, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Brunel's shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

What is Brunel's FEI number?

Brunel's FDA Establishment Identifier (FEI) is 3015935741.