Heiltropfen Lab
FDA import alert and refusal historyMarkovci, SloveniaFEI 3017429916
Recorded by FDA as HEILTROPFEN LAB
As of October 26, 2026, Heiltropfen Lab is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines 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
- Classified NAI (No Action Indicated)
Every FDA record for Heiltropfen Lab
3 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
- Import refusalSource
Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry EAY-0039754-2Show 2 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry EAY-0039754-2Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry EAY-0039754-2Source
Refusal charges, in plain English
- 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 Heiltropfen Lab
- Is Heiltropfen Lab on an FDA import alert?
- No listing for Heiltropfen Lab 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 Lab?
- Yes. FDA refused 2 shipment lines from Heiltropfen Lab 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 Lab's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- When was Heiltropfen Lab last inspected by FDA?
- FDA's most recent inspection of Heiltropfen Lab with a final classification is dated August 29, 2023 and was classified NAI (No Action Indicated).
- What is Heiltropfen Lab's FEI number?
- Heiltropfen Lab's FDA Establishment Identifier (FEI) is 3017429916.
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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.