FDA Inspection 1108422 — Tusker Medical, Inc.

Tusker Medical, Inc. — FEI 3012130335

The FDA completed an inspection of Tusker Medical, Inc. on October 25, 2019 in Menlo Park, 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
October 25, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Menlo Park, CA (United States)