FDA Inspection 982333 — GlaxoSmithKline Manufacturing S.P.A.

GlaxoSmithKline Manufacturing S.P.A. — FEI 3002807114

The FDA completed an inspection of GlaxoSmithKline Manufacturing S.P.A. on Jul 22, 2016 in Torrile. 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
Jul 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Torrile (Italy)

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