ADM WILD Europe GmbH & Co. KG
FDA import alert and refusal historyBerlin, GermanyFEI 3009925785
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
- Import alerts
- IA 45-02 · red list
- 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
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 45-02red listWoodruff Color TypeSource
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).
Buying from ADM WILD Europe GmbH & Co. KG?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.