FDA Inspection 735204 — GlaxoSmithKline Manufacturing S.P.A.

GlaxoSmithKline Manufacturing S.P.A. — FEI 3002807114

The FDA completed an inspection of GlaxoSmithKline Manufacturing S.P.A. on Jun 28, 2011 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
Jun 28, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Torrile (Italy)

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