Dectro Intl., Inc. FDA Record
- No warning letters matched by name
Dectro Intl., Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Dectro Intl., Inc." is on file.
- Latest 510(k)
- Jan 12, 1995
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 | 1 | 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 |
|---|---|---|
| K943928 | APILUS ELECTROPIL | Jan 12, 1995 |
Dectro Intl., Inc. and the FDA: common questions
Has Dectro Intl., Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Dectro Intl., Inc." 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 Dectro Intl., Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Dectro Intl., Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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