FDA Inspection 1160001 — Nemaura Pharma Limited

Nemaura Pharma Limited — FEI 3019640628

The FDA completed an inspection of Nemaura Pharma Limited on Dec 10, 2021 in Loughborough. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

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

Additional Details

Sponsor, Contract Research Organization

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.