FDA Inspection
Microlight Corporation of AmericaMicrolight Corporation of America – FDA Inspection, Sep 6, 2018
Record Details
This FDA Inspection record concerns Microlight Corporation of America, with an inspection on September 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · fdf9c5d6-a1a2-42d9-869a-e7a94e4f37af
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059120
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Microlight Corporation of America
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 24, 2025 | NAI | Dallas District Office | Postmarket Assurance: Medical Devices |
Other documents for Microlight Corporation of America
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.