# Source-Ray Inc., Ronkonkoma, NY – FDA Inspections

Source: https://www.keypedia.com/companies/source-ray-inc/a1a0d5fe-0223-4259-b0e1-75cf501f1d65

> Inspection records and compliance data for Source-Ray Inc. in Ronkonkoma, New York. 7 FDA inspections on record, 2 Form 483s, last inspected February 07, 2023.

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## Details

- Name: Source-Ray Inc.
- FEI Number: 3004606964
- Address Line 1: 50 Fleetwood Ct
- City: Ronkonkoma
- State: New York
- Zip Code: 11779
- Country Name: United States
- Address: 50 Fleetwood Ct, Ronkonkoma, New York 11779, United States
- Country: United States

## Related Documents

- FDA Inspection 1197354 - Source-Ray Inc. - 2023-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2023
- FDA Inspection 1092603 - Source-Ray Inc. - 2019-05-28 — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2019
- [FDA Inspection 1107855 - Source-Ray Inc. - 2018-11-02](https://www.keypedia.com/records/fda_inspections/source-ray-inc/70581097-6d97-4220-8443-14260087c050) — source: FDA, date: November 2, 2018
- FDA Inspection 1029491 - Source-Ray Inc. - 2017-10-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2017
- [FDA Inspection 1029491 - Source-Ray Inc. - 2017-10-19](https://www.keypedia.com/records/fda_inspections/source-ray-inc/6c80eb32-ac51-4ff1-a9e4-bb3abb9f9603) — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2017
- FDA Inspection 893522 - Source-Ray Inc. - 2014-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2014
- FDA Inspection 893522 - Source-Ray Inc. - 2014-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2014
- FDA Inspection 893522 - Source-Ray Inc. - 2014-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2014
- FDA Inspection 792768 - Source-Ray Inc. - 2012-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2012
- FDA Inspection 792768 - Source-Ray Inc. - 2012-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2012

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