Establishment registration
MEDICAL DEVICE POST-PRODUCTION SERVICES, INC.
FDA establishment registration 3012849830 · Poway, US
Key facts
| Registration number | 3012849830 |
|---|---|
| Establishment name | MEDICAL DEVICE POST-PRODUCTION SERVICES, INC. |
| Owner/operator | Medical Device Post-Production Services, Inc. |
| Owner/operator number | 10052730 |
| FEI number | 3012849830 |
| Address | 16405 Summer Sage Rd |
| City | Poway |
| State | CA |
| 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