Establishment registration
HORIBA ABX SAS
FDA establishment registration 3000148879 · MONTPELLIER Herault, FR
Key facts
| Registration number | 3000148879 |
|---|---|
| Establishment name | HORIBA ABX SAS |
| Owner/operator | HORIBA ABX SAS |
| Owner/operator number | 9036328 |
| FEI number | 3000148879 |
| Address | PARC EUROMEDECINE |
| City | MONTPELLIER Herault |
| Country | FR |
| Establishment types | Complaint file establishment, Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | CDQ, CDT, CEK, CEM, CEO, CFJ, CFN, CFR, CGS, CGX, CGZ, CHH, CHI, CIC, CIG, CIT, CIX, CJE, CJY, CKA, CZP, DBF, DCF, DCK, DDG, DDR, DEW, DFT, DHR, GGK and 33 more |
| Device classes | 1, 2 |
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