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Provithor B.V.

FDA import alert and refusal historyVolkel, NetherlandsFEI 3017123448

Recorded by FDA as PROVITHOR B.V.

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Example subjectProvithor B.V added to Import Alert 16-129 (red list)

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As of October 25, 2026, Provithor B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on September 9, 2020, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Provithor B.V.

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

2020

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-1444534-2
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-1434488-3
    Source

Refusal charges, in plain English

  • UNAPPROVED2 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.

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 2 shipment lines from Provithor B.V. on September 9, 2020. The most recent, on September 9, 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 charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Provithor B.V.'s FEI number?
Provithor B.V.'s FDA Establishment Identifier (FEI) is 3017123448.

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Example subjectProvithor B.V added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.