Establishment registration
A. SCHWEICKHARDT GMBH & CO. KG
FDA establishment registration 8010159 · Seitingen-Oberflacht Baden-Wurttemberg, DE
Key facts
| Registration number | 8010159 |
|---|---|
| Establishment name | A. SCHWEICKHARDT GMBH & CO. KG |
| Owner/operator | ADOLF SCHWEICKHARDT GMBH & CO. KG |
| Owner/operator number | 8010159 |
| FEI number | 1000390051 |
| Address | Tuttlinger Str. 12 |
| City | Seitingen-Oberflacht Baden-Wurttemberg |
| Country | DE |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | DZN, EAX, ECB, ECP, ECR, ECS, EFL, EGN, EHK, EHY, EIG, EIK, EIL, EIR, EIS, EIX, EIY, EJB, EJG, EJY, EKB, EKC, EKD, EKE, EKG, EKH, EKI, EKJ, EKK, EKR and 34 more |
| Device classes | 1 |
At a glance
- 10–99 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