# Sunlight Medical, Inc. – FDA Inspection, Oct 26, 2018

Source: https://www.keypedia.com/records/fda_inspections/sunlight-medical-inc/d009ed33-53c0-447f-99a5-06c0bd1e9ecd
Source feed: FDA_Inspections

> FDA inspection 1070153 of Sunlight Medical, Inc., October 26, 2018. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070153
- Company Name: Sunlight Medical, Inc.
- Inspection Date: 2018-10-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

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- FDA Inspection 778475 - 2012-04-18

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/sunlight-medical-inc/bb61e75e-27de-4671-a6e3-31c3747b8069

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