Remia C.V.

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

Refusal charges, in plain English

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• 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 Remia C.V.

Is Remia C.V. on an FDA import alert?

No listing for Remia C.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 Remia C.V.?

Yes. FDA refused 2 shipment lines from Remia C.V. between March 22, 2017 and April 13, 2020. The most recent, on April 13, 2020, was condiments, n.e.c., charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse Remia C.V.'s shipments?

The most frequent charges are NO ENGLISH (required label information not in english, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

When was Remia C.V. last inspected by FDA?

FDA's most recent inspection of Remia C.V. with a final classification is dated October 17, 2019 and was classified NAI (No Action Indicated).

What is Remia C.V.'s FEI number?

Remia C.V.'s FDA Establishment Identifier (FEI) is 3009850743.