Establishment registration
ACME-MONACO CORP.
FDA establishment registration 1222301 · PRESQUE ISLE, US
Key facts
| Registration number | 1222301 |
|---|---|
| Establishment name | ACME-MONACO CORP. |
| Owner/operator | ACME-MONACO CORP. |
| Owner/operator number | 1293141 |
| FEI number | 1000121071 |
| Address | 1450 Central Drive |
| City | PRESQUE ISLE |
| State | ME |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DQX, DRB, DZC, ECN, ECO, EJF |
| Device classes | 1, 2 |
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