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Eu Supplements

FDA import alert and refusal historyBunnik, NetherlandsFEI 3012197834

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Example subjectEu Supplement added to Import Alert 16-129 (red list)

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As of October 26, 2026, Eu Supplements is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between October 21, 2016 and October 25, 2016, 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. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Eu Supplements

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

2016

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0416740-0
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIRECTIONSUNAPPROVEDEntry UPS-0414644-6
    Source
  3. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0416842-4
    Source
  4. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTHEALTH CUNAPPROVEDEntry UPS-0416692-3
    Source
  5. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry UPS-0414656-0
    Source
  6. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0434121-1
    Source

Refusal charges, in plain English

  • UNAPPROVED6 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.

  • FILTHY4 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • HEALTH C4 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.

  • NCONTACT4 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.

  • 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.

  • DIRECTIONS1 refused line

    DIRECTIONS

Questions about Eu Supplements

Is Eu Supplements on an FDA import alert?
No listing for Eu Supplements 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 Eu Supplements?
Yes. FDA refused 6 shipment lines from Eu Supplements between October 21, 2016 and October 25, 2016. The most recent, on October 25, 2016, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Eu Supplements's shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 6 lines) and FILTHY (filthy, putrid or decomposed substance, 4 lines).
What is Eu Supplements's FEI number?
Eu Supplements's FDA Establishment Identifier (FEI) is 3012197834.

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Example subjectEu Supplement 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.