FDA Inspection 1089069 — Clearpath Surgical, Inc.
The FDA completed an inspection of Clearpath Surgical, Inc. on March 20, 2019 in Palo Alto, 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
- March 20, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Palo Alto, CA (United States)