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FDA Inspection 846300 — Grand River Aseptic Manufacturing, Inc.

Grand River Aseptic Manufacturing, Inc. — FEI 3008716173

The FDA completed an inspection of Grand River Aseptic Manufacturing, Inc. on August 28, 2013 in Grand Rapids, MI. 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
August 28, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Rapids, MI (United States)

Facility

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  • 1145269 (VAI Fri Jul 02 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060743 (NAI Wed Jun 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources