Establishment registration
SANZAY CORPORATION -
FDA establishment registration 3005146313 · Miami Gardens, US
Key facts
| Registration number | 3005146313 |
|---|---|
| Establishment name | SANZAY CORPORATION - |
| Owner/operator | Sanzay Corporation - Integrated Diagnostics Group |
| Owner/operator number | 10026301 |
| FEI number | 3005146313 |
| Address | 1080 NW 163rd Drive |
| City | Miami Gardens |
| State | FL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDM, CDQ, CDT, CEI, CEJ, CEK, CEM, CEN, CEO, CET, CFB, CFJ, CFR, CGA, CGS, CGX, CGZ, CHH, CHJ, CIC, CIG, CIT, CIX, CJE, CJJ, CKB, DCF, DCK, DHR, DIH and 36 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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