Tanita Corporation Of America FDA Record
- No warning letters matched by name
Tanita Corporation Of America has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Tanita Corporation Of America" is on file.
- Latest 510(k)
- Jul 7, 2009
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 | 2 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 0 | 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 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K090479 | TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 | Jul 7, 2009 |
| K062652 | INNERSCAN BODY COMPOSITION MONITOR, INNERSCAN SEGMENTAL BODY COMPOSITION MONITOR | Dec 28, 2006 |
Tanita Corporation Of America and the FDA: common questions
Has Tanita Corporation Of America received an FDA warning letter?
No FDA warning letter addressed to the name "Tanita Corporation Of America" 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 Tanita Corporation Of America received an FDA Form 483?
FDA has not published a Form 483 for "Tanita Corporation Of America" in its reading room. FDA publishes some Form 483s, not all of them.
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