Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.
FDA import alert and refusal historyElburg, NetherlandsFEI 1000392920
As of October 26, 2026, Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. (Elburg, Netherlands) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for thyme, whole (spice), 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listThyme, Whole (Spice)Source
Questions about Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.
- Is Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. on an FDA import alert?
- Yes. As of October 26, 2026, Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for thyme, whole (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.?
- No FDA import refusals for Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.'s FEI number?
- Verenigde Nederlandse Kruidendrogerijen (VNK) B.V.'s FDA Establishment Identifier (FEI) is 1000392920.
- Can shipments from Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. still enter the U.S.?
- Shipments of thyme, whole (spice) from Verenigde Nederlandse Kruidendrogerijen (VNK) B.V. can be detained without physical examination under Import Alert 99-19; 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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