# FDA Inspection 1059120 - Microlight Corporation of America - September 06, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/microlight-corporation-of-america/fdf9c5d6-a1a2-42d9-869a-e7a94e4f37af/
Source feed: FDA_Inspections

> FDA Inspection 1059120 for Microlight Corporation of America on September 06, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059120
- Company Name: Microlight Corporation of America
- Inspection Date: 2018-09-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/microlight-corporation-of-america/836a7125-9dee-4835-9b1f-86b8ccc5ac45

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