vanRijsingeningredients B.V.

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 vanRijsingeningredients B.V.

Is vanRijsingeningredients B.V. on an FDA import alert?

No listing for vanRijsingeningredients 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 vanRijsingeningredients B.V.?

Yes. FDA refused 1 shipment line from vanRijsingeningredients B.V. on August 31, 2022. The most recent, on August 31, 2022, was carrot (root & tuber vegetable), charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse vanRijsingeningredients B.V.'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 vanRijsingeningredients B.V. last inspected by FDA?

FDA's most recent inspection of vanRijsingeningredients B.V. with a final classification is dated January 23, 2025 and was classified NAI (No Action Indicated).

What is vanRijsingeningredients B.V.'s FEI number?

vanRijsingeningredients B.V.'s FDA Establishment Identifier (FEI) is 3013773437.