SupplierRadar

vitOrgan Arzneimittel GmbH

FDA import alert and refusal historyOstfildern, GermanyFEI 1000461726

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on vitOrgan Arzneimittel GmbH.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectvitOrgan Arzneimittel Gmb added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, vitOrgan Arzneimittel GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 12 of its shipment lines on September 3, 2024, most often for dietary ingredients not listed (DIETARYING).

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. · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for vitOrgan Arzneimittel GmbH

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

2024

  1. Import refusal
    Refused, 12 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRELACKS FIRMDIETARYINGNCONTACTEntry ENM-9231747-8Show 12 lines
    Source

Refusal charges, in plain English

  • DIETARYING10 refused lines

    Dietary ingredients not listed

    The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.

  • LABELING10 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.

  • LACKS FIRM10 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LIST INGRE10 refused lines

    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).

  • NCONTACT10 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 LBL10 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.

  • NO ENGLISH2 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • 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 vitOrgan Arzneimittel GmbH

Is vitOrgan Arzneimittel GmbH on an FDA import alert?
No listing for vitOrgan Arzneimittel GmbH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from vitOrgan Arzneimittel GmbH?
Yes. FDA refused 12 shipment lines from vitOrgan Arzneimittel GmbH on September 3, 2024. The most recent, on September 3, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse vitOrgan Arzneimittel GmbH's shipments?
The most frequent charges are DIETARYING (dietary ingredients not listed, 10 lines) and LABELING (fair packaging and labeling act, 10 lines).
What is vitOrgan Arzneimittel GmbH's FEI number?
vitOrgan Arzneimittel GmbH's FDA Establishment Identifier (FEI) is 1000461726.

Buying from vitOrgan Arzneimittel GmbH?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on vitOrgan Arzneimittel GmbH.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectvitOrgan Arzneimittel Gmb added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.