Vermeulen Mechelen
FDA import alert and refusal historyNetherlands, NetherlandsFEI 3005210786
As of October 26, 2026, Vermeulen Mechelen (Netherlands, Netherlands) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for brussels sprouts (leaf & stem vegetable), raw, fresh, ambient; brussels sprouts (leaf & stem vegetable), raw, fresh, refrigerated, published by FDA on September 16, 2009, 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 Vermeulen Mechelen
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listBrussels Sprouts (Leaf & Stem Vegetable), Raw, Fresh, Ambient; Brussels Sprouts (Leaf & Stem Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Vermeulen Mechelen
- Is Vermeulen Mechelen on an FDA import alert?
- Yes. As of October 26, 2026, Vermeulen Mechelen is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for brussels sprouts (leaf & stem vegetable), raw, fresh, ambient; brussels sprouts (leaf & stem vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Vermeulen Mechelen?
- No FDA import refusals for Vermeulen Mechelen appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Vermeulen Mechelen's FEI number?
- Vermeulen Mechelen's FDA Establishment Identifier (FEI) is 3005210786.
- Can shipments from Vermeulen Mechelen still enter the U.S.?
- Shipments of brussels sprouts (leaf & stem vegetable), raw, fresh, ambient; brussels sprouts (leaf & stem vegetable), raw, fresh, refrigerated from Vermeulen Mechelen 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.