# AlcoPro Inc

FEI: 1000112835
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: AlcoPro Inc (#10033291)

Address: 1626 Downtown West Boulevard, Knoxville, TN, US



## Products

Total registered: 1
Top product codes: DJZ
Regulation §: 862.3050

Proprietary names: BreathIQ, Alco-Breath Tube, CheckPoint

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000112835%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000112835