Amp 2024 Usfda. Showing 1 to 23 of 23. The usfda conducted the inspection from 9 september 2024 to 13 september 2024.
The manufacturer and user facility device experience (maude) database is a searchable database of medical device reports (mdrs) of adverse events involving medical devices. The usfda conducted the inspection from 9 september 2024 to 13 september 2024.