FDA Inspection 1160001 — Nemaura Pharma Limited

Nemaura Pharma Limited — FEI 3019640628

The FDA completed an inspection of Nemaura Pharma Limited on December 10, 2021 in Loughborough. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 10, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Loughborough (United Kingdom)

Additional Details

Sponsor, Contract Research Organization