Establishment registration
American Laboratory Products Company
FDA establishment registration 1222302 · Salem, US
Key facts
| Registration number | 1222302 |
|---|---|
| Establishment name | American Laboratory Products Company |
| Owner/operator | AMERICAN LABORATORY PRODUCTS CO., LTD. |
| Owner/operator number | 9000664 |
| FEI number | 1000121039 |
| Address | 26 Keewaydin Drive |
| City | Salem |
| State | NH |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDP, CDZ, CEP, CEW, CFL, CFP, CFT, CGF, CGI, CGJ, CHP, CIZ, CKG, DEG, DGC, GGT, GPF, JHI, JKC, JKD, JKR, JLS, JLX, JMD, JME, JNG, JNN, KLI, LJM, LLL and 8 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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