Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1873955910
Device Listing 1873955910
Listing Summary
#
Listing key
1873955910
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
94384
3007309299
3007309299
Kent McKesson
1
N
2026-01-01
300 N Alloy DR Fenton Fenton MI US 48430