Delka, S.A.

2 records, 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 Delka, S.A.

Is Delka, S.A. on an FDA import alert?

No listing for Delka, 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 Belgium page.

Has FDA refused shipments from Delka, S.A.?

Yes. FDA refused 1 shipment line from Delka, S.A. on September 14, 2021. The most recent, on September 14, 2021, was sauces, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Delka, S.A.'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).

When was Delka, S.A. last inspected by FDA?

FDA's most recent inspection of Delka, S.A. with a final classification is dated February 12, 2025 and was classified NAI (No Action Indicated).

What is Delka, S.A.'s FEI number?

Delka, S.A.'s FDA Establishment Identifier (FEI) is 3013471777.