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FDA Inspection 988732 — Avista Pharma Solutions, Inc.

Avista Pharma Solutions, Inc. — FEI 1220785

The FDA completed an inspection of Avista Pharma Solutions, Inc. on June 15, 2016 in Agawam, MA. 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
June 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Agawam, MA (United States)

Facility

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  • 1113974 (VAI Wed Dec 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1067530 (NAI Wed Sep 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850250 (VAI Fri Sep 27 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 696758 (NAI Wed Oct 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources