483
Maynard R. Rasmussen, M.DMaynard R. Rasmussen, M.D – FDA 483, May 6, 2022
Record Details
An FDA inspection of Maynard R. Rasmussen, M.D. in San Diego, CA, a clinical investigator, identified an issue with investigational drug disposition records. The firm failed to adequately document the dates and quantities for unused maintenance doses of study drug kits for multiple subjects. This indicates a deficiency in accountability for investigational products.
View Company Profile
ID · 88496dfd-f2e5-4d0b-8c70-8dc380f7402c
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.