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
1020622371
Device Listing 1020622371
Listing Summary
#
Listing key
1020622371
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
20067
3002731203
3002731203
Jon Ward
1
N
2020-04-25
11705 Boyette Road Suite 503 Riverview FL US 33569