FDA Inspection 1017435 — RXSight Inc.

RXSight Inc. — FEI 3012712027

The FDA completed an inspection of RXSight Inc. on June 29, 2017 in Aliso Viejo, 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
June 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Aliso Viejo, CA (United States)