# FDA Inspection 837252 - Sharplight Technologies - June 13, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/sharplight-technologies/642a7fb5-8b92-45ff-869d-3c452bcb4c7a
Source feed: FDA_Inspections

> FDA Inspection 837252 for Sharplight Technologies on June 13, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 837252
- Company Name: Sharplight Technologies
- Inspection Date: 2013-06-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1082722 - 2019-02-14](https://www.globalkeysolutions.net/records/fda_inspections/sharplight-technologies/024259d1-fa30-46c1-be38-a44bb0cd2e16)
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- [FDA Inspection 837252 - 2013-06-13](https://www.globalkeysolutions.net/records/fda_inspections/sharplight-technologies/e2fbd3d0-3f8e-4116-bfd0-aa9d79748827)

Company: https://www.globalkeysolutions.net/companies/sharplight-technologies/2a49963e-5486-407c-87af-d14606822794

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7