FDA Inspection 1080947 — SleepMe Inc
The FDA completed an inspection of SleepMe Inc on Dec 12, 2018 in Pittsburgh, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 12, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Pittsburgh, PA (United States)