FDA Inspection 659061 — SkyePharma Production SAS

SkyePharma Production SAS — FEI 3002808180

The FDA completed an inspection of SkyePharma Production SAS on Apr 2, 2010 in St Quentin Fallavier. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 2, 2010
Fiscal Year
2010
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.