Establishment registration
ALMIKRO GMBH & CO. KG
FDA establishment registration 3009134855 · Bad Krozingen Baden-Wurttemberg, DE
Key facts
| Registration number | 3009134855 |
|---|---|
| Establishment name | ALMIKRO GMBH & CO. KG |
| Owner/operator | Almikro GmbH & Co. KG |
| Owner/operator number | 10057705 |
| FEI number | 3009134855 |
| Address | Loewenweg 1e |
| City | Bad Krozingen Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | EOB, FGB, GCJ, HET, HFA, MNL |
| Device classes | 1, 2, f |
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