FDA Inspection 1017485 — Dr. Alexey Manikhas

Dr. Alexey Manikhas — FEI 3008459953

The FDA completed an inspection of Dr. Alexey Manikhas on April 28, 2017 in Sankt-Peterburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sankt-Peterburg (Russia)

Additional Details

Clinical Investigator (CI)