FDA Inspection 1117960 — Michael Kos MD

Michael Kos MD — FEI 3015685131

The FDA completed an inspection of Michael Kos MD on December 19, 2019 in Reno, NV. 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
December 19, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Reno, NV (United States)

Additional Details

Clinical Investigator (CI)