# LIQUIPAK CORP.

FEI: 1815703
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: LIQUIPAK CORP. (#1815703)

Address: 2205 REDMAN DRIVE, Alma, MI, US



## Products

Total registered: 1
Top product codes: LRJ
Regulation §: 880.6890

Proprietary names: Vesta-Syde Decontamination System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221815703%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1815703