Morinda International Tahiti FDA Record
- Latest inspection VAI · May 25, 2016
- No warning letters matched by name
Morinda International Tahiti has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Morinda International Tahiti" is on file.
- Latest inspection
- May 25, 2016 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 1 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| May 25, 2016 | Mataiea, France | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3008403419 |
- 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 3008403419 | Mataiea, France | 1 | May 25, 2016 |
Morinda International Tahiti and the FDA: common questions
Has Morinda International Tahiti received an FDA warning letter?
No FDA warning letter addressed to the name "Morinda International Tahiti" 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 Morinda International Tahiti received an FDA Form 483?
FDA has not published a Form 483 for "Morinda International Tahiti" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Morinda International Tahiti?
The most recent FDA inspection on file ended May 25, 2016 at Mataiea, France and was classified VAI. FDA has 1 inspection of Morinda International Tahiti on file.
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