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Dayonix Pharma GmbH - Portugal

FDA import alert and refusal historyLisbon, PortugalFEI 3015225671

Recorded by FDA as DAYONIX PHARMA GMBH - PORTUGAL

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Example subjectDayonix Pharma GmbH - Portuga added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dayonix Pharma GmbH - Portugal is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on April 18, 2019, most often for unauthorized nutrient content or health claim (HEALTH C).

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

Every FDA record for Dayonix Pharma GmbH - Portugal

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

2019

  1. Import refusal
    Refused, 3 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTLABELINGNUTRIT LBLHEALTH CEntry SCS-4092710-6Show 3 lines
    Source

Refusal charges, in plain English

  • HEALTH C3 refused lines

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • LABELING3 refused lines

    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.

  • NCONTACT3 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 LBL3 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.

  • 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.

Questions about Dayonix Pharma GmbH - Portugal

Is Dayonix Pharma GmbH - Portugal on an FDA import alert?
No listing for Dayonix Pharma GmbH - Portugal appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
Has FDA refused shipments from Dayonix Pharma GmbH - Portugal?
Yes. FDA refused 3 shipment lines from Dayonix Pharma GmbH - Portugal on April 18, 2019. The most recent, on April 18, 2019, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
Why did FDA refuse Dayonix Pharma GmbH - Portugal's shipments?
The most frequent charges are HEALTH C (unauthorized nutrient content or health claim, 3 lines) and LABELING (fair packaging and labeling act, 3 lines).
What is Dayonix Pharma GmbH - Portugal's FEI number?
Dayonix Pharma GmbH - Portugal's FDA Establishment Identifier (FEI) is 3015225671.

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Example subjectDayonix Pharma GmbH - Portuga 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.