# LaserSight Technologies, Inc., Winter Park, FL – FDA Inspections

Source: https://www.keypedia.com/companies/lasersight-technologies-inc/e8e51aa5-f2d8-4138-96fa-c93c0eb7349d

> Inspection records and compliance data for LaserSight Technologies, Inc. in Winter Park, Florida. 3 FDA inspections on record, last inspected February 02, 2012.

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## Details

- Name: LaserSight Technologies, Inc.
- FEI Number: 3002741596
- Address Line 1: 931 S. Semoran Boulevard
- City: Winter Park
- State: Florida
- Zip Code: 32792
- Country Name: United States
- Address: 931 S. Semoran Boulevard, Winter Park, Florida 32792, United States
- Country: United States

## Related Documents

- [FDA Inspection 765704 - LaserSight Technologies, Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/lasersight-technologies-inc/b446e9e4-b92d-4182-9b4a-2adc7d150b78) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2012
- FDA Inspection 765705 - LaserSight Technologies, Inc. - 2012-02-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2012
- [FDA Inspection 765705 - LaserSight Technologies, Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/lasersight-technologies-inc/c2c91a1b-1de4-4709-ab63-4c61283754c0) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012
- FDA Inspection 765705 - LaserSight Technologies, Inc. - 2012-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012
- FDA Inspection 562131 - LaserSight Technologies, Inc. - 2009-01-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2009
- [FDA Inspection 562131 - LaserSight Technologies, Inc. - 2009-01-21](https://www.keypedia.com/records/fda_inspections/lasersight-technologies-inc/ee2123c8-5bda-4dab-b08a-d5bb729f7412) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2009
- FDA Inspection 562131 - LaserSight Technologies, Inc. - 2009-01-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2009

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