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ABNOBA GmbH

FDA import alert and refusal historyNiefern-Oschelbronn, GermanyFEI 3026811998

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

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As of October 26, 2026, ABNOBA GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between May 23, 2023 and July 29, 2026, 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
Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for ABNOBA GmbH

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

2026

  1. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry AEK-0467705-9
    Source
  2. Import refusal
    Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-0842062-1
    Source
  3. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry AEK-9184766-3
    Source

2025

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NOT LISTEDFRNMFGREGEntry AEK-7761944-1
    Source

2023

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-3239243-1
    Source

Refusal charges, in plain English

  • UNAPPROVED4 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.

  • FRNMFGREG1 refused line

    FRNMFGREG

  • NOT LISTED1 refused line

    Product not listed with FDA

    The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

Questions about ABNOBA GmbH

Is ABNOBA GmbH on an FDA import alert?
No listing for ABNOBA 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 ABNOBA GmbH?
Yes. FDA refused 5 shipment lines from ABNOBA GmbH between May 23, 2023 and July 29, 2026. The most recent, on July 29, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse ABNOBA GmbH's shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and FRNMFGREG (frnmfgreg, 1 line).
What is ABNOBA GmbH's FEI number?
ABNOBA GmbH's FDA Establishment Identifier (FEI) is 3026811998.

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Example subjectABNOBA Gmb 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.