De Wijndragers B.V

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

Refusal charges, in plain English

• NEEDS FCE8 refused lines

  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 PROCESS8 refused lines

  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 De Wijndragers B.V

Is De Wijndragers B.V on an FDA import alert?

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

Has FDA refused shipments from De Wijndragers B.V?

Yes. FDA refused 8 shipment lines from De Wijndragers B.V on May 29, 2026. The most recent, on May 29, 2026, was sauces, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse De Wijndragers B.V's shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 8 lines) and NO PROCESS (no scheduled process filed, 8 lines).

When was De Wijndragers B.V last inspected by FDA?

FDA's most recent inspection of De Wijndragers B.V with a final classification is dated February 12, 2015 and was classified VAI (Voluntary Action Indicated).

What is De Wijndragers B.V's FEI number?

De Wijndragers B.V's FDA Establishment Identifier (FEI) is 3009872866.