Eurowest
FDA import alert and refusal historyPoeldijk, NetherlandsFEI 3012705012
Recorded by FDA as EUROWEST
As of October 26, 2026, Eurowest is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 21, 2016, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Brussels sprouts (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Eurowest
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Eurowest
- Is Eurowest on an FDA import alert?
- No listing for Eurowest appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from Eurowest?
- Yes. FDA refused 1 shipment line from Eurowest on December 21, 2016. The most recent, on December 21, 2016, was brussels sprouts (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Eurowest's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Eurowest's FEI number?
- Eurowest's FDA Establishment Identifier (FEI) is 3012705012.
Buying from Eurowest?
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.