FDA Inspection 1210490 — Ruben D. Kowalyszyn, MD

Ruben D. Kowalyszyn, MD — FEI 3027239040

The FDA completed an inspection of Ruben D. Kowalyszyn, MD on July 14, 2023 in Viedma. 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
July 14, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Viedma (Argentina)

Additional Details

Clinical Investigator (CI)