SupplierRadar

Heiltropfen

FDA import alert and refusal historyPtujptuj, SloveniaFEI 3012098365

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Heiltropfen.

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

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

Free for one supplier. No password, no card.

As of October 26, 2026, Heiltropfen is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 8, 2023, 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. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Heiltropfen

1 record, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry EAY-0039754-2
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    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 Heiltropfen

Is Heiltropfen on an FDA import alert?
No listing for Heiltropfen appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Slovenia page.
Has FDA refused shipments from Heiltropfen?
Yes. FDA refused 1 shipment line from Heiltropfen on June 8, 2023. The most recent, on June 8, 2023, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Heiltropfen's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Heiltropfen's FEI number?
Heiltropfen's FDA Establishment Identifier (FEI) is 3012098365.

Buying from Heiltropfen?

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 Heiltropfen.

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

Example subjectHeiltropfe 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.