van der arden
FDA import alert and refusal historyPijnakker, NetherlandsFEI 2000018784
As of October 25, 2026, van der arden (Pijnakker, Netherlands) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for leeks, published by FDA on July 11, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for van der arden
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-05red listLeeksSource
Questions about van der arden
- Is van der arden on an FDA import alert?
- Yes. As of October 25, 2026, van der arden is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for leeks; FDA published the listing on July 11, 2014.
- Has FDA refused shipments from van der arden?
- No FDA import refusals for van der arden appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is van der arden's FEI number?
- van der arden's FDA Establishment Identifier (FEI) is 2000018784.
- Can shipments from van der arden still enter the U.S.?
- Shipments of leeks from van der arden can be detained without physical examination under Import Alert 99-05; 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.