FDA Inspection 1042884 — Precision Spine Inc
The FDA completed an inspection of Precision Spine Inc on August 11, 2017 in Pearl, MS. 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
- August 11, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Pearl, MS (United States)