Establishment registration
GERMAINE LABORATORIES, INC.
FDA establishment registration 1649661 · SAN ANTONIO, US
Key facts
| Registration number | 1649661 |
|---|---|
| Establishment name | GERMAINE LABORATORIES, INC. |
| Owner/operator | GERMAINE LABORATORIES, INC. |
| Owner/operator number | 9031523 |
| FEI number | 3001451797 |
| Address | 11030 Wye Drive |
| City | SAN ANTONIO |
| State | TX |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | CDM, CEN, CEP, CGA, CHH, CIG, DCN, DHA, DHR, DIC, DIF, DIO, DIS, DJG, DJR, DJZ, DKZ, DSF, GGM, GKR, GMQ, GNC, GRL, GRM, GSK, GSL, GSM, GSN, GSO, GSY and 49 more |
| Device classes | 1, 2, N, U |
At a glance
- 10–99 Device listings
- 1,000+ 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