# FDA Inspection 1179919 - LENSAR, Inc. - September 21, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/de6769ae-3c5e-417d-921d-99373d0c7125
Source feed: FDA_Inspections

> FDA Inspection 1179919 for LENSAR, Inc. on September 21, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179919
- Company Name: LENSAR, Inc.
- Inspection Date: 2022-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179919 - 2022-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/3060adc7-567a-49c7-9ca3-7804d5f65733)
- [FDA Inspection 1179919 - 2022-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/46e2c927-5456-48b0-8471-f0215d6c890e)
- [FDA Inspection 970534 - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/b3451e00-00cf-433d-9f45-1c1270a8c71f)
- [FDA Inspection 970534 - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/a94ac264-f6ea-49b3-9a3d-f7ffc6ad2321)
- [FDA Inspection 970534 - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/7f2ff55f-a22c-4fa9-969d-130d35142564)

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

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