Dms Products, Inc. FDA Record
- No warning letters matched by name
Dms Products, Inc. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Dms Products, Inc." is on file.
- Latest 510(k)
- Nov 9, 1989
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 | 6 | 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 |
|---|---|---|
| K891004 | RAPIDEC STAPH | Nov 9, 1989 |
| K894805 | RAPIDEC UR | Sep 26, 1989 |
| K890626 | RAPIDEC COLI | Jun 2, 1989 |
| K890625 | JAMES REAGENT | Feb 17, 1989 |
| K854733 | API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT) | Mar 6, 1986 |
| K854732 | API 50 CHB (CULTURE MEDIA) | Mar 4, 1986 |
Dms Products, Inc. and the FDA: common questions
Has Dms Products, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Dms Products, 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 Dms Products, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Dms Products, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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