FDA Inspection 1268673 — Sever Pharma Solutions

Sever Pharma Solutions — FEI 3004620701

The FDA completed an inspection of Sever Pharma Solutions on May 12, 2023 in Malmo. 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
May 12, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Malmo (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)