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SANUM-Kehlbeck GmbH & Co. KG

FDA import alert and refusal historyHoya, GermanyFEI 3002128313

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Example subjectSANUM-Kehlbeck GmbH & Co. K added to Import Alert 16-129 (red list)

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As of October 26, 2026, SANUM-Kehlbeck GmbH & Co. KG is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between February 6, 2024 and July 8, 2026, most often for drug gmps (DRUG GMPS).

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. · DRUG GMPS
Last warning letter
None found
Last inspection
None on record

Every FDA record for SANUM-Kehlbeck GmbH & Co. KG

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

2026

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DRUG GMPSEntry 1FX-8854744-2
    Source

2025

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.SUPPL GMPEntry SCS-2244237-6
    Source

2024

  1. Import refusal
    Refused, Citrus aurantium ( herbal & botanical other than teas)UNAPPROVEDEntry SCS-1866265-4
    Source

Refusal charges, in plain English

  • DRUG GMPS1 refused line

    DRUG GMPS

  • SUPPL GMP1 refused line

    Dietary supplement CGMP not met

    The product appeared to be a dietary supplement prepared, packed, or held under conditions that do not meet current good manufacturing practice (CGMP) regulations.

  • 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 SANUM-Kehlbeck GmbH & Co. KG

Is SANUM-Kehlbeck GmbH & Co. KG on an FDA import alert?
No listing for SANUM-Kehlbeck GmbH & Co. KG 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 SANUM-Kehlbeck GmbH & Co. KG?
Yes. FDA refused 3 shipment lines from SANUM-Kehlbeck GmbH & Co. KG between February 6, 2024 and July 8, 2026. The most recent, on July 8, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as DRUG GMPS (drug gmps).
Why did FDA refuse SANUM-Kehlbeck GmbH & Co. KG's shipments?
The most frequent charges are DRUG GMPS (drug gmps, 1 line) and SUPPL GMP (dietary supplement cgmp not met, 1 line).
What is SANUM-Kehlbeck GmbH & Co. KG's FEI number?
SANUM-Kehlbeck GmbH & Co. KG's FDA Establishment Identifier (FEI) is 3002128313.

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Example subjectSANUM-Kehlbeck GmbH & Co. K 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.