Doehler Neuenkirchen GmbH
FDA import alert and refusal historyOtterndorf, GermanyFEI 3013289092
As of October 26, 2026, Doehler Neuenkirchen GmbH (Otterndorf, Germany) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for elderberry juice, published by FDA on June 20, 2013, 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 Doehler Neuenkirchen GmbH
2 records, newest first. Each line links to the FDA page it came from.
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 99-08red listElderberry JuiceSource
Questions about Doehler Neuenkirchen GmbH
- Is Doehler Neuenkirchen GmbH on an FDA import alert?
- Yes. As of October 26, 2026, Doehler Neuenkirchen GmbH is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for elderberry juice; FDA published the listing on June 20, 2013.
- Has FDA refused shipments from Doehler Neuenkirchen GmbH?
- No FDA import refusals for Doehler Neuenkirchen GmbH appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Doehler Neuenkirchen GmbH last inspected by FDA?
- FDA's most recent inspection of Doehler Neuenkirchen GmbH with a final classification is dated February 10, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Doehler Neuenkirchen GmbH's FEI number?
- Doehler Neuenkirchen GmbH's FDA Establishment Identifier (FEI) is 3013289092.
- Can shipments from Doehler Neuenkirchen GmbH still enter the U.S.?
- Shipments of elderberry juice from Doehler Neuenkirchen 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.