# LENSAR, Inc. - Inspection Records

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

> Inspection records and compliance data for LENSAR, Inc. in Orlando, Florida. Access full analysis and detailed observations.

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## Details

- Name: LENSAR, Inc.
- FEI Number: 3009026057
- City: Orlando
- State: Florida
- Country Name: United States
- Address Line 1: 2800 Discovery Dr Ste 100
- Zip Code: 32826

## Related Documents

- [FDA Inspection 1315508 - LENSAR, Inc. - 2026-04-16](https://www.keypedia.com/records/fda_inspections/lensar-inc/a6dc5967-62d6-4ab4-a485-a55a5ddc1194) — source: FDA, date: April 16, 2026
- [483 - LENSAR, Inc. - 2022-09-21](https://www.keypedia.com/records/483/lensar-inc/929bf968-304c-4cbe-8930-73f63a82afc6) — source: FDA, date: September 21, 2022
- [FDA Inspection 1179919 - LENSAR, Inc. - 2022-09-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/3060adc7-567a-49c7-9ca3-7804d5f65733) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2022
- [FDA Inspection 1179919 - LENSAR, Inc. - 2022-09-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/46e2c927-5456-48b0-8471-f0215d6c890e) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2022
- [FDA Inspection 1179919 - LENSAR, Inc. - 2022-09-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/de6769ae-3c5e-417d-921d-99373d0c7125) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2022
- [FDA Inspection 970534 - LENSAR, Inc. - 2016-05-24](https://www.keypedia.com/records/fda_inspections/lensar-inc/b3451e00-00cf-433d-9f45-1c1270a8c71f) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 970534 - LENSAR, Inc. - 2016-05-24](https://www.keypedia.com/records/fda_inspections/lensar-inc/a94ac264-f6ea-49b3-9a3d-f7ffc6ad2321) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 970534 - LENSAR, Inc. - 2016-05-24](https://www.keypedia.com/records/fda_inspections/lensar-inc/7f2ff55f-a22c-4fa9-969d-130d35142564) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 825456 - LENSAR, Inc. - 2013-03-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/c08d0a11-7392-496f-892c-f4ad6abdaaf1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013
- [FDA Inspection 825456 - LENSAR, Inc. - 2013-03-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/de83fb45-dc0b-447b-85e4-8228cfcadfa2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013
- [FDA Inspection 825456 - LENSAR, Inc. - 2013-03-21](https://www.keypedia.com/records/fda_inspections/lensar-inc/f8691810-795b-4e0d-965f-3be5e9fc7b44) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013

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