Provithor B.V.

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

Refusal charges, in plain English

• UNAPPROVED3 refused lines

  Unapproved new drug

  The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Provithor B.V.

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

No listing for Provithor B.V. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.

Has FDA refused shipments from Provithor B.V.?

Yes. FDA refused 3 shipment lines from Provithor B.V. between August 7, 2020 and September 23, 2020. The most recent, on September 23, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Provithor B.V.'s shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 3 lines) and LACKS FIRM (manufacturer name and address missing, 1 line).

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

Provithor B.V.'s FDA Establishment Identifier (FEI) is 3016790065.