# Medical Laser Systems Inc - Inspection Records

Source: https://www.keypedia.com/companies/medical-laser-systems-inc/06c730f4-df4a-40b4-8669-c4c68399cf3b

> Inspection records and compliance data for Medical Laser Systems Inc in Branford, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Medical Laser Systems Inc
- FEI Number: 3006157902
- City: Branford
- State: Connecticut
- Country Name: United States
- Address Line 1: 20 Baldwin Dr
- Zip Code: 06405

## Related Documents

- [FDA Inspection 970159 - Medical Laser Systems Inc - 2016-05-11](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/c60d7a3d-bcca-4e31-9064-110c68ba53c8) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2016
- [FDA Inspection 970159 - Medical Laser Systems Inc - 2016-05-11](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/5fb9424c-0c09-4473-a010-e6c3cbe0fc93) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2016
- [FDA Inspection 970159 - Medical Laser Systems Inc - 2016-05-11](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/cff3646b-d5cd-4bad-a625-af3f6cd82537) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2016
- [FDA Inspection 836812 - Medical Laser Systems Inc - 2013-06-17](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/53592338-fde2-4555-8444-edda26aa0896) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 17, 2013
- [FDA Inspection 836812 - Medical Laser Systems Inc - 2013-06-17](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/e9cdd2dc-2d80-4302-b61c-a7366c999f29) — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2013
- [FDA Inspection 700970 - Medical Laser Systems Inc - 2010-12-14](https://www.keypedia.com/records/fda_inspections/medical-laser-systems-inc/12ed86eb-5a49-4f23-a7d5-1c7200154807) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2010

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