Kaasmakerij Henri Willig B.V.
FDA import alert and refusal historyHeerenveen, NetherlandsFEI 3004270525
As of October 26, 2026, Kaasmakerij Henri Willig B.V. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 26, 2013, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kaasmakerij Henri Willig B.V.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Kaasmakerij Henri Willig B.V.
- Is Kaasmakerij Henri Willig B.V. on an FDA import alert?
- No listing for Kaasmakerij Henri Willig 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 Kaasmakerij Henri Willig B.V.?
- No FDA import refusals for Kaasmakerij Henri Willig B.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kaasmakerij Henri Willig B.V. last inspected by FDA?
- FDA's most recent inspection of Kaasmakerij Henri Willig B.V. with a final classification is dated August 26, 2013 and was classified NAI (No Action Indicated).
- What is Kaasmakerij Henri Willig B.V.'s FEI number?
- Kaasmakerij Henri Willig B.V.'s FDA Establishment Identifier (FEI) is 3004270525.
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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.