FDA Inspection 1179682 — Oculus Surgical Inc

Oculus Surgical Inc — FEI 3009773841

The FDA completed an inspection of Oculus Surgical Inc on August 31, 2022 in Port Saint Lucie, FL. 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
August 31, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Port Saint Lucie, FL (United States)