FDA Inspection 1105498 — SkyePharma Production SAS

SkyePharma Production SAS — FEI 3002808180

The FDA completed an inspection of SkyePharma Production SAS on September 6, 2019 in St Quentin Fallavier. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
St Quentin Fallavier (France)