# FDA Inspection 984850 - Kaylight Corporation - September 12, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaylight-corporation/fa995cd6-9cb0-4b35-9a3e-2d309af1bf67/
Source feed: FDA_Inspections

> FDA Inspection 984850 for Kaylight Corporation on September 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984850
- Company Name: Kaylight Corporation
- Inspection Date: 2016-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/kaylight-corporation/07ab8b52-572e-44aa-9243-9203180b05c0

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