Establishment registration
GOLDEN MAX LLC
FDA establishment registration 1000595987 · Missouri City, US
Key facts
| Registration number | 1000595987 |
|---|---|
| Establishment name | GOLDEN MAX LLC |
| Owner/operator | Golden Max LLC |
| Owner/operator number | 10087901 |
| FEI number | 1000595987 |
| Address | 525 S. Cravens Rd., Suite 100 |
| City | Missouri City |
| State | TX |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | FPA |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 100–999 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