Dohler Sp. z o.o.
FDA import alert and refusal historyBelsk Duzy, PolandFEI 3006349594
As of October 26, 2026, Dohler Sp. z o.o. (Belsk Duzy, Poland) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for strawberries dried or paste, published by FDA on February 6, 2014, 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 Dohler Sp. z o.o.
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 99-08red listStrawberries Dried or PasteSource
Questions about Dohler Sp. z o.o.
- Is Dohler Sp. z o.o. on an FDA import alert?
- Yes. As of October 26, 2026, Dohler Sp. z o.o. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for strawberries dried or paste; FDA published the listing on February 6, 2014.
- Has FDA refused shipments from Dohler Sp. z o.o.?
- No FDA import refusals for Dohler Sp. z o.o. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Dohler Sp. z o.o. last inspected by FDA?
- FDA's most recent inspection of Dohler Sp. z o.o. with a final classification is dated November 7, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Dohler Sp. z o.o.'s FEI number?
- Dohler Sp. z o.o.'s FDA Establishment Identifier (FEI) is 3006349594.
- Can shipments from Dohler Sp. z o.o. still enter the U.S.?
- Shipments of strawberries dried or paste from Dohler Sp. z o.o. 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.