FDA Inspection 984449 — PainDx, Inc.
The FDA completed an inspection of PainDx, Inc. on June 8, 2016 in Laguna Beach, CA. 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
- June 8, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Laguna Beach, CA (United States)