FDA inspection
Microlight Corporation of America: FDA inspection ending Sep 6, 2018
FDA inspection 1059120 · Voluntary Action Indicated (VAI) · Missouri City, TX
Key facts
| Inspection ID | 1059120 |
|---|---|
| Firm | Microlight Corporation of America |
| FEI number | 3003654318 |
| Address | 333 Southwestern Blvd Ste 208 |
| City | Missouri City |
| State | TX |
| ZIP | 77459 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Sep 6, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data