Ernteband Fruchtsaft GmbH
FDA import alert and refusal historyWinnenden, GermanyFEI 3004251045
As of October 26, 2026, Ernteband Fruchtsaft GmbH (Winnenden, Germany) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for strawberry puree, published by FDA on August 1, 2022, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Ernteband Fruchtsaft GmbH
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-08red listStrawberry PureeSource
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Ernteband Fruchtsaft GmbH
- Is Ernteband Fruchtsaft GmbH on an FDA import alert?
- Yes. As of October 26, 2026, Ernteband Fruchtsaft GmbH is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for strawberry puree; FDA published the listing on August 1, 2022.
- Has FDA refused shipments from Ernteband Fruchtsaft GmbH?
- No FDA import refusals for Ernteband Fruchtsaft GmbH appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Ernteband Fruchtsaft GmbH last inspected by FDA?
- FDA's most recent inspection of Ernteband Fruchtsaft GmbH with a final classification is dated March 21, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Ernteband Fruchtsaft GmbH's FEI number?
- Ernteband Fruchtsaft GmbH's FDA Establishment Identifier (FEI) is 3004251045.
- Can shipments from Ernteband Fruchtsaft GmbH still enter the U.S.?
- Shipments of strawberry puree from Ernteband Fruchtsaft GmbH can be detained without physical examination under Import Alert 99-08; 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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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.