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
1035183013
Device Listing 1035183013
Listing Summary
#
Listing key
1035183013
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
75202
2025917
2025917
NEOTECH PRODUCTS, LLC
1
N
2026-01-01
28430 Witherspoon Pkwy Valencia CA US 91355