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FDA Inspection 972358 — Acist Medical Systems

Acist Medical Systems — FEI 3001726808

The FDA completed an inspection of Acist Medical Systems on March 1, 2016 in Eden Prairie, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 1, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)

Facility

Other inspections at this facility

  • 1166885 (NAI Mon Feb 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1081356 (NAI Mon Mar 04 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 783932 (NAI Wed Jun 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 654321 (NAI Wed Mar 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources