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Lowensenf GmbH

FDA import alert and refusal historyDusseldorf, GermanyFEI 3009479567

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

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As of October 26, 2026, Lowensenf GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 10 of its shipment lines between May 4, 2017 and September 14, 2022, most often for required label information not in english (NO ENGLISH).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vegetable & vegetable products not mentioned elsewhere, n.e.c. · NEEDS ACID
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Lowensenf GmbH

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

2022

  1. Import refusal
    Refused, 3 lines in one entry: Vegetable & vegetable products not mentioned elsewhere, n.e.c.NEEDS ACIDNEEDS FCENO PROCESSEntry U52-1805710-2Show 3 lines
    Source

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2017

  1. Import refusal
    Refused, 7 lines in one entry: Mustard, preparedNO ENGLISHEntry U52-7720994-1Show 7 lines
    Source

Refusal charges, in plain English

  • NO ENGLISH7 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.

  • NEEDS FCE3 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO PROCESS2 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • NEEDS ACID1 refused line

    NEEDS ACID

Questions about Lowensenf GmbH

Is Lowensenf GmbH on an FDA import alert?
No listing for Lowensenf 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 Lowensenf GmbH?
Yes. FDA refused 10 shipment lines from Lowensenf GmbH between May 4, 2017 and September 14, 2022. The most recent, on September 14, 2022, was vegetable & vegetable products not mentioned elsewhere, n.e.c., charged as NEEDS ACID (needs acid).
Why did FDA refuse Lowensenf GmbH's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 7 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 3 lines).
When was Lowensenf GmbH last inspected by FDA?
FDA's most recent inspection of Lowensenf GmbH with a final classification is dated December 18, 2018 and was classified NAI (No Action Indicated).
What is Lowensenf GmbH's FEI number?
Lowensenf GmbH's FDA Establishment Identifier (FEI) is 3009479567.

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Example subjectLowensenf 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.