Establishment registration
LANSINOH LABORATORIES, INC.
FDA establishment registration 2032361 · ALEXANDRIA, US
Key facts
| Registration number | 2032361 |
|---|---|
| Establishment name | LANSINOH LABORATORIES, INC. |
| Owner/operator | LANSINOH LABORATORIES, INC. |
| Owner/operator number | 9045862 |
| FEI number | 3022898 |
| Address | 99 Canal Center Plaza, Alexandria, Suite 550 |
| City | ALEXANDRIA |
| State | VA |
| Country | US |
| Registration valid through | 2026 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None 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