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FDA Inspection 1233170 — Grand River Aseptic Manufacturing, Inc.

Grand River Aseptic Manufacturing, Inc. — FEI 3008716173

The FDA completed an inspection of Grand River Aseptic Manufacturing, Inc. on February 21, 2024 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 21, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1293364 (VAI Tue Nov 04 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 955644 (NAI Thu Dec 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904415 (VAI Mon Nov 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources