Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3009026057.
Observations1
Issue DateSeptember 21, 2022
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
LENSAR, Inc.
Location
Orlando, Florida, United States
FEI Number
3009026057
Product Type
Devices
Issue Date
September 21, 2022
Country
United States
Inspection History, 2013 to 2026
NAI2
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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