FDA Inspection 1101272 — Vimta Labs, Limited

Vimta Labs, Limited — FEI 3005580517

The FDA completed an inspection of Vimta Labs, Limited on August 16, 2019 in Hyderabad. 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
August 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Hyderabad (India)

Additional Details

Clinical BA/BE