# Microlight Corporation of America – FDA Inspection, Sep 6, 2018

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

> FDA inspection 1059120 of Microlight Corporation of America, September 06, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1251436 - 2025-01-24](https://www.keypedia.com/records/fda_inspections/microlight-corporation-of-america/a921a8b5-42fc-4966-9cbe-e39ab160acce)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jocelyn-c-turner/7e39f6e0-9750-4460-8a4e-27ee9306b77e)

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

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