Keema And Co. FDA Record
Keema And Co. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Keema And Co." is on file.
- Latest 510(k)
- Nov 30, 1994
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 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 |
|---|---|---|
| K924502 | REUSABLE MENSTRUAL PAD | Nov 30, 1994 |
Keema And Co. and the FDA: common questions
Has Keema And Co. received an FDA warning letter?
No FDA warning letter addressed to the name "Keema And Co." 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 Keema And Co. received an FDA Form 483?
FDA has not published a Form 483 for "Keema And Co." in its reading room. FDA publishes some Form 483s, not all of them.
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