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FDA Inspection 1060743 — Grand River Aseptic Manufacturing, Inc.

Grand River Aseptic Manufacturing, Inc. — FEI 3008716173

The FDA completed an inspection of Grand River Aseptic Manufacturing, Inc. on June 20, 2018 in Grand Rapids, MI. 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
June 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Rapids, MI (United States)

Facility

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  • 1233170 (VAI Wed Feb 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1145269 (VAI Fri Jul 02 2021 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