GREENYEARD PREPARED NETHERLANDSBV FDA Record
GREENYEARD PREPARED NETHERLANDSBV has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "GREENYEARD PREPARED NETHERLANDSBV" is on file.
- Latest inspection
- Feb 13, 2015 · OAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Feb 13, 2015 | Horst, Netherlands | Food/Cosmetics | Official Action Indicated (OAI) | 3002808932 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3002808932 | Horst, Netherlands | 1 | Feb 13, 2015 |
GREENYEARD PREPARED NETHERLANDSBV and the FDA: common questions
Has GREENYEARD PREPARED NETHERLANDSBV received an FDA warning letter?
No FDA warning letter addressed to the name "GREENYEARD PREPARED NETHERLANDSBV" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has GREENYEARD PREPARED NETHERLANDSBV received an FDA Form 483?
FDA has not published a Form 483 for "GREENYEARD PREPARED NETHERLANDSBV" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect GREENYEARD PREPARED NETHERLANDSBV?
The most recent FDA inspection on file ended Feb 13, 2015 at Horst, Netherlands and was classified OAI. FDA has 1 inspection of GREENYEARD PREPARED NETHERLANDSBV on file, 1 of them classified OAI (official action indicated).
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