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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 June 28, 2011 in Torrile. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 28, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Torrile (Italy)

Facility

Other inspections at this facility

  • 1244033 (VAI Thu Oct 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1064045 (VAI Fri Sep 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 982333 (NAI Fri Jul 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934049 (VAI Wed May 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 842545 (NAI Wed Jul 10 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

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