FDA Inspection 1085854 — Trimedyne Inc

Trimedyne Inc — FEI 1419951

The FDA completed an inspection of Trimedyne Inc on March 21, 2019 in Corona, 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 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Corona, CA (United States)