FDA Inspection 1009142 — Sunny Hussain

Sunny Hussain — FEI 3013321044

The FDA completed an inspection of Sunny Hussain on April 6, 2017 in Shreveport, LA. 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 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shreveport, LA (United States)

Additional Details

Clinical Investigator (CI)