FDA Inspection 1223661 — Techfit Digital Surgery Inc

Techfit Digital Surgery Inc — FEI 3016560308

The FDA completed an inspection of Techfit Digital Surgery Inc on Nov 10, 2023 in Daytona Beach, FL. 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
Nov 10, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Daytona Beach, FL (United States)