FDA inspection
Mlife Diagnostics LLC: FDA inspection ending May 14, 2025
FDA inspection 1271106 · Voluntary Action Indicated (VAI) · Marshall, TX
Key facts
| Inspection ID | 1271106 |
|---|---|
| Firm | Mlife Diagnostics LLC |
| FEI number | 3017060097 |
| Address | 511 N Washington Ave |
| City | Marshall |
| State | TX |
| ZIP | 75670-2007 |
| Fiscal year | 2025 |
| Inspection end date | May 14, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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