FDA Inspection 1115347 — Uplevity, Inc.
The FDA completed an inspection of Uplevity, Inc. on January 15, 2020 in Niantic, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 15, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Niantic, CT (United States)