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FDA Inspection 842545 — GlaxoSmithKline Manufacturing S.p.A.

GlaxoSmithKline Manufacturing S.p.A. — FEI 3002807114

The FDA completed an inspection of GlaxoSmithKline Manufacturing S.p.A. on July 10, 2013 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
July 10, 2013
Fiscal Year
2013
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))
  • 801922 (NAI Fri Sep 21 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources