FDA Inspection 1120318 — BSolve Limited

BSolve Limited — FEI 3008847596

The FDA completed an inspection of BSolve Limited on November 21, 2019 in Glasgow. 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
November 21, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glasgow (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)