# Light Sources, Inc., Orange, CT – FDA Inspections

Source: https://www.keypedia.com/companies/light-sources-inc/1c1cfea7-8574-4399-a670-5a344487281d

> Inspection records and compliance data for Light Sources, Inc. in Orange, Connecticut. 4 FDA inspections on record, 1 Form 483, last inspected September 19, 2023.

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## Details

- Name: Light Sources, Inc.
- FEI Number: 1221013
- Address Line 1: 37 Robinson Blvd
- City: Orange
- State: Connecticut
- Zip Code: 06477
- Country Name: United States
- Address: 37 Robinson Blvd, Orange, Connecticut 06477, United States
- Country: United States

## Related Documents

- FDA Inspection 1218118 - Light Sources, Inc. - 2023-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2023
- [FDA Inspection 1218118 - Light Sources, Inc. - 2023-09-19](https://www.keypedia.com/records/fda_inspections/light-sources-inc/b8d24f7f-624f-4d1f-b1a2-2d601f6888c6) — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2023
- FDA Inspection 1218118 - Light Sources, Inc. - 2023-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2023
- FDA Inspection 1070748 - Light Sources, Inc. - 2018-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2018
- FDA Inspection 1070748 - Light Sources, Inc. - 2018-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2018
- FDA Inspection 1070748 - Light Sources, Inc. - 2018-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2018
- FDA Inspection 950878 - Light Sources, Inc. - 2015-11-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 17, 2015
- FDA Inspection 950878 - Light Sources, Inc. - 2015-11-17 — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2015
- FDA Inspection 950878 - Light Sources, Inc. - 2015-11-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 17, 2015
- FDA Inspection 824154 - Light Sources, Inc. - 2013-03-25 — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2013

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