FDA Inspection 1179919 — LENSAR, Inc.

LENSAR, Inc. — FEI 3009026057

The FDA completed an inspection of LENSAR, Inc. on September 21, 2022 in Orlando, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 21, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Orlando, FL (United States)

Citations

IDCFRDescription
570021 CFR 1002.10Failure to submit, distinct marking