FDA Inspection 1017391 — Dr. Rubin H. Saavedra

Dr. Rubin H. Saavedra — FEI 3007207754

The FDA completed an inspection of Dr. Rubin H. Saavedra on June 16, 2017 in Las Vegas, NV. 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
June 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Las Vegas, NV (United States)

Additional Details

Clinical Investigator (CI)