FDA 483 - Ann Moore, FNP-C - May 30, 2025

Ann Moore, FNP-C in Peoria, AZ, was inspected from May 27-30, 2025, and received a Form 483. The inspection revealed a failure to maintain adequate case histories for clinical trial subjects. Specifically, required examination records for two subjects with Type 2 Diabetes were not retrieved and reviewed, hindering the assessment of subject safety and potential adverse events.