Eu Supplements
FDA import alert and refusal historyBunnik, NetherlandsFEI 3012197834
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
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0416740-0Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIRECTIONSUNAPPROVEDEntry UPS-0414644-6Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0416842-4Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTHEALTH CUNAPPROVEDEntry UPS-0416692-3Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry UPS-0414656-0Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYNCONTACTLABELINGHEALTH CUNAPPROVEDEntry UPS-0434121-1Source
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.
Buying from Eu Supplements?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.