Veembedrijf A. Buisman B.V.
FDA import alert and refusal historyZwolle, NetherlandsFEI 3013321125
As of October 26, 2026, Veembedrijf A. Buisman B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 15, 2022, 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
- Gluten, wheat · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Veembedrijf A. Buisman B.V.
2 records, 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 Veembedrijf A. Buisman B.V.
- Is Veembedrijf A. Buisman B.V. on an FDA import alert?
- No listing for Veembedrijf A. Buisman B.V. 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 Veembedrijf A. Buisman B.V.?
- Yes. FDA refused 1 shipment line from Veembedrijf A. Buisman B.V. on March 15, 2022. The most recent, on March 15, 2022, was gluten, wheat, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Veembedrijf A. Buisman B.V.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- When was Veembedrijf A. Buisman B.V. last inspected by FDA?
- FDA's most recent inspection of Veembedrijf A. Buisman B.V. with a final classification is dated January 19, 2026 and was classified NAI (No Action Indicated).
- What is Veembedrijf A. Buisman B.V.'s FEI number?
- Veembedrijf A. Buisman B.V.'s FDA Establishment Identifier (FEI) is 3013321125.
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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.