Kwekerij Mooijman BV
FDA import alert and refusal historyNootdorp, NetherlandsFEI 3015234907
As of October 26, 2026, Kwekerij Mooijman BV has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 19, 2019, 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 Kwekerij Mooijman BV
2 records, newest first. Each line links to the FDA page it came from.
Questions about Kwekerij Mooijman BV
- Is Kwekerij Mooijman BV on an FDA import alert?
- No listing for Kwekerij Mooijman BV 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 Kwekerij Mooijman BV?
- No FDA import refusals for Kwekerij Mooijman BV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kwekerij Mooijman BV last inspected by FDA?
- FDA's most recent inspection of Kwekerij Mooijman BV with a final classification is dated June 19, 2019 and was classified NAI (No Action Indicated).
- What is Kwekerij Mooijman BV's FEI number?
- Kwekerij Mooijman BV's FDA Establishment Identifier (FEI) is 3015234907.
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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.