Establishment registration
LOUISVILLE APL DIAGNOSTICS, INC.
FDA establishment registration 1529254 · Texas City, US
Key facts
| Registration number | 1529254 |
|---|---|
| Establishment name | LOUISVILLE APL DIAGNOSTICS, INC. |
| Owner/operator | LOUISVILLE APL DIAGNOSTICS, INC. |
| Owner/operator number | 9008974 |
| FEI number | 1000305932 |
| Address | 702 9TH ST N STE A |
| City | Texas City |
| State | TX |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | MID, MSV |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database