FDA Inspection 838912 — SkyePharma Production SAS

SkyePharma Production SAS — FEI 3002808180

The FDA completed an inspection of SkyePharma Production SAS on May 31, 2013 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
May 31, 2013
Fiscal Year
2013
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.