Establishment registration
MDF INSTRUMENTS DIRECT, INC.
FDA establishment registration 3005374305 · Westlake Village, US
Key facts
| Registration number | 3005374305 |
|---|---|
| Establishment name | MDF INSTRUMENTS DIRECT, INC. |
| Owner/operator | MDF INSTRUMENTS DIRECT, INC. |
| Owner/operator number | 9078563 |
| FEI number | 3005374305 |
| Address | 1014 S Westlake Blvd |
| City | Westlake Village |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
At a glance
- 1–9 Device listings
- None 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