# FDA Inspection 825456 - LENSAR, Inc. - March 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/lensar-inc/f8691810-795b-4e0d-965f-3be5e9fc7b44
Source feed: FDA_Inspections

> FDA Inspection 825456 for LENSAR, Inc. on March 21, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 825456
- Company Name: LENSAR, Inc.
- Inspection Date: 2013-03-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/lensar-inc/768e79dd-d0c9-4b28-8219-e188878bb08b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7