Sckoon, Inc.
Sckoon, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent FDA inspection ended on Feb 9, 2015 (Voluntary Action Indicated (VAI)). Its most recent 510(k) clearance was granted on Sep 18, 2012.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Feb 9, 2015 | Miami, FL | Devices | Voluntary Action Indicated (VAI) | 3009843022 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K120107 | SCKOONCUP | Sep 18, 2012 |