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ADM WILD Europe GmbH & Co. KG

FDA import alert and refusal historyBerlin, GermanyFEI 3009925785

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Example subjectADM WILD Europe GmbH & Co. K added to Import Alert 16-129 (red list)

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As of October 26, 2026, ADM WILD Europe GmbH & Co. KG (Berlin, Germany) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for woodruff color type, published by FDA on June 26, 2015, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for ADM WILD Europe GmbH & Co. KG

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

2022

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2015

  1. Import alert listing
    Listed on Import Alert 45-02red listWoodruff Color Type
    Source

Questions about ADM WILD Europe GmbH & Co. KG

Is ADM WILD Europe GmbH & Co. KG on an FDA import alert?
Yes. As of October 26, 2026, ADM WILD Europe GmbH & Co. KG is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for woodruff color type; FDA published the listing on June 26, 2015.
Has FDA refused shipments from ADM WILD Europe GmbH & Co. KG?
No FDA import refusals for ADM WILD Europe GmbH & Co. KG appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was ADM WILD Europe GmbH & Co. KG last inspected by FDA?
FDA's most recent inspection of ADM WILD Europe GmbH & Co. KG with a final classification is dated August 17, 2022 and was classified NAI (No Action Indicated).
What is ADM WILD Europe GmbH & Co. KG's FEI number?
ADM WILD Europe GmbH & Co. KG's FDA Establishment Identifier (FEI) is 3009925785.
Can shipments from ADM WILD Europe GmbH & Co. KG still enter the U.S.?
Shipments of woodruff color type from ADM WILD Europe GmbH & Co. KG can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectADM WILD Europe 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.