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Provero Pharma B.V.

FDA import alert and refusal historySchijndel, NetherlandsFEI 3014229766

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

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As of October 26, 2026, Provero Pharma B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between May 10, 2019 and July 31, 2024, most often for no u.s. adverse event contact on supplement label (NCONTACT).

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. · LABELING
Last warning letter
None found
Last inspection
None on record

Every FDA record for Provero Pharma B.V.

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

2024

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LABELINGNUTRIT LBLEntry 9G3-0207807-2
    Source

2023

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENCONTACTEntry 9G3-0196645-9
    Source

2019

  1. Import refusal
    Refused, 4 lines in one entry: Herbals & botanicals (not teas), n.e.c.NCONTACTNUTRIT LBLDIETARYLBLFALSEEntry SCS-4220898-4Show 4 lines
    Source

Refusal charges, in plain English

  • NCONTACT5 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • NUTRIT LBL5 refused lines

    Nutrition information missing from label

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

  • DIETARYLBL1 refused line

    Not identified as a dietary supplement

    The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Provero Pharma B.V.

Is Provero Pharma B.V. on an FDA import alert?
No listing for Provero Pharma 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 Provero Pharma B.V.?
Yes. FDA refused 6 shipment lines from Provero Pharma B.V. between May 10, 2019 and July 31, 2024. The most recent, on July 31, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LABELING (fair packaging and labeling act).
Why did FDA refuse Provero Pharma B.V.'s shipments?
The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 5 lines) and NUTRIT LBL (nutrition information missing from label, 5 lines).
What is Provero Pharma B.V.'s FEI number?
Provero Pharma B.V.'s FDA Establishment Identifier (FEI) is 3014229766.

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Example subjectProvero Pharma 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.