# CITEST DIAGNOSTICS INC.

FEI: 3023296261
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Citest Diagnostics Inc. (#10090628)

Address: 170-422, RICHARDS ST, VANCOUVER British Columbia, V6B 2Z4, CA

Mandatory US Agent: ACESO LABORATORIES INC.

## Products

Total registered: 23
Top product codes: LDJ, LCM, NFW, NGL, NFY, JXM, NGM, LAF, DJG, PTG, LFG, DKZ, NFV, DIS, NFT, DIO, NGG, DNK, DJC, DJR
Regulation §: 862.3870, 862.3650, 862.3250, 862.3170, 862.3610, 862.3620, 862.3910, 862.3100, 862.3150, 862.3640

Proprietary names: Citest Multiplex DOA Home Test Cup (Urine), Citest Multiplex DOA Home Test Panel (Urine), Citest Multiplex DOA Test Panel (Urine), Citest Multiplex DOA Test Cup (Urine)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223023296261%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3023296261