FDA Inspection 1115347 — Uplevity, Inc.
The FDA completed an inspection of Uplevity, Inc. on Jan 15, 2020 in Niantic, CT. 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
- Jan 15, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Niantic, CT (United States)