FDA Inspection 1203360 — Timothy E. Ritter, MD

Timothy E. Ritter, MD — FEI 3014958741

The FDA completed an inspection of Timothy E. Ritter, MD on March 30, 2023 in Southlake, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 30, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Southlake, TX (United States)

Additional Details

Clinical Investigator (CI)