FDA Inspection 1013960 — Jitrenda Gandhi

Jitrenda Gandhi — FEI 3013355931

The FDA completed an inspection of Jitrenda Gandhi on June 1, 2017 in Morristown, TN. 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
June 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Morristown, TN (United States)

Additional Details

Clinical Investigator (CI)