# ACTIONPAK, INC.

FEI: 3002303857
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: ActionPak, Inc. (#10043895)

Address: 1600 River Avenue, Camden, NJ, US



## Products

Total registered: 1
Top product codes: OCH
Regulation §: 870.2700

Proprietary names: Pulse Oximeter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002303857%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002303857