FDA Inspection 938881 — SkyePharma Production SAS

SkyePharma Production SAS — FEI 3002808180

The FDA completed an inspection of SkyePharma Production SAS on Jun 19, 2015 in St Quentin Fallavier. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 19, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
St Quentin Fallavier (France)

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