Cantoliva S.A.

2 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• 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 Cantoliva S.A.

Is Cantoliva S.A. on an FDA import alert?

No listing for Cantoliva S.A. 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 Cantoliva S.A.?

Yes. FDA refused 1 shipment line from Cantoliva S.A. on January 13, 2026. The most recent, on January 13, 2026, was vegetable & vegetable products not mentioned elsewhere, n.e.c., charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse Cantoliva S.A.'s shipments?

The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).

When was Cantoliva S.A. last inspected by FDA?

FDA's most recent inspection of Cantoliva S.A. with a final classification is dated April 10, 2026 and was classified VAI (Voluntary Action Indicated).

What is Cantoliva S.A.'s FEI number?

Cantoliva S.A.'s FDA Establishment Identifier (FEI) is 3004702983.