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Gutfeeling Labs AB

FDA import alert and refusal historyLund, SwedenFEI 3030429098

Recorded by FDA as GUTFEELING LABS AB

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Example subjectGutfeeling Labs A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gutfeeling Labs AB is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 18, 2024, most often for nutrition information missing from label (NUTRIT LBL).

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

Current status

Import alerts
Not listed
Last import refusal
Dietary conventional foods, n.e.c. · NUTRIT LBL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gutfeeling Labs AB

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

2024

  1. Import refusal
    Refused, Dietary conventional foods, n.e.c.NUTRIT LBLEntry AEK-4842612-4
    Source

Refusal charges, in plain English

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Gutfeeling Labs AB

Is Gutfeeling Labs AB on an FDA import alert?
No listing for Gutfeeling Labs AB appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Sweden page.
Has FDA refused shipments from Gutfeeling Labs AB?
Yes. FDA refused 1 shipment line from Gutfeeling Labs AB on March 18, 2024. The most recent, on March 18, 2024, was dietary conventional foods, n.e.c., charged as NUTRIT LBL (nutrition information missing from label).
Why did FDA refuse Gutfeeling Labs AB's shipments?
The most frequent charge is NUTRIT LBL (nutrition information missing from label, 1 line).
What is Gutfeeling Labs AB's FEI number?
Gutfeeling Labs AB's FDA Establishment Identifier (FEI) is 3030429098.

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Example subjectGutfeeling Labs A 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.