Home / Inspections / 955644

FDA Inspection 955644 — Grand River Aseptic Manufacturing, Inc.

Grand River Aseptic Manufacturing, Inc. — FEI 3008716173

The FDA completed an inspection of Grand River Aseptic Manufacturing, Inc. on December 3, 2015 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
December 3, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
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))
  • 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))
  • 1060743 (NAI Wed Jun 20 2018 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