Establishment registration
Acero Precision
FDA establishment registration 3000170817 · West Chester, US
Key facts
| Registration number | 3000170817 |
|---|---|
| Establishment name | Acero Precision |
| Owner/operator | ACERO PRECISION |
| Owner/operator number | 9072046 |
| FEI number | 3000170817 |
| Address | 1340 Enterprise Drive |
| City | West Chester |
| State | PA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | HRS, HWC, KWP, KWQ, MAX, MNH, MNI, MQP, MRW, NKB, NKG, ODP, OSH, OUR, OVD, OVE |
| Device classes | 2, U |
At a glance
- 100–999 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