FDA Inspection 1095043 — Timothy E. Ritter, MD

Timothy E. Ritter, MD — FEI 3014958741

The FDA completed an inspection of Timothy E. Ritter, MD on May 23, 2019 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
May 23, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Southlake, TX (United States)

Additional Details

Clinical Investigator (CI)