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FDA Inspection 1100246 — Hospira Australia Pty Ltd.

Hospira Australia Pty Ltd. — FEI 3001174929

The FDA completed an inspection of Hospira Australia Pty Ltd. on July 2, 2019 in Mulgrave. 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 2, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mulgrave (Australia)

Facility

Other inspections at this facility

  • 1181593 (VAI Fri Sep 02 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 945591 (NAI Tue Sep 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 869582 (OAI Tue Mar 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737223 (VAI Mon Mar 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 612891 (NAI Tue Aug 25 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources