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FDA Inspection 1009606 — Shionogi Pharma Co., Ltd.

Shionogi Pharma Co., Ltd. — FEI 3002808135

The FDA completed an inspection of Shionogi Pharma Co., Ltd. on September 16, 2016 in Isawa-Gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Isawa-Gun (Japan)

Facility

Other inspections at this facility

  • 1275087 (OAI Tue Jul 01 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1069417 (NAI Fri Sep 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1009607 (NAI Fri Sep 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 874759 (VAI Tue Apr 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 772467 (NAI Thu Feb 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources