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

Source: https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/de83fb45-dc0b-447b-85e4-8228cfcadfa2
Source feed: FDA_Inspections

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

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 825456
- Company Name: LENSAR, Inc.
- Inspection Date: 2013-03-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- 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 1179919 - 2022-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lensar-inc/de6769ae-3c5e-417d-921d-99373d0c7125)
- [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)

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