FDA Inspection 1098673 — Plamen Popivanov

Plamen Popivanov — FEI 3015357441

The FDA completed an inspection of Plamen Popivanov on July 24, 2019 in Sofia. 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 24, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sofia (Bulgaria)

Additional Details

Clinical Investigator (CI)