FDA Inspection 840796 — Jacques Hebert MD

Jacques Hebert MD — FEI 3007826115

The FDA completed an inspection of Jacques Hebert MD on July 19, 2013 in Quebec. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 19, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Quebec (Canada)

Additional Details

Clinical Investigator (CI)