FDA Inspection 1059120 — Microlight Corporation Of America
The FDA completed an inspection of Microlight Corporation Of America on Sep 6, 2018 in Missouri City, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 6, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Missouri City, TX (United States)