FDA Inspection 1265624 — SkyePharma Production SAS

SkyePharma Production SAS — FEI 3002808180

The FDA completed an inspection of SkyePharma Production SAS on October 27, 2023 in St Quentin Fallavier. 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
October 27, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
St Quentin Fallavier (France)

Additional Details

Mutual Recognition Agreement (MRA)