FDA Inspection 1081356 — Acist Medical Systems

Acist Medical Systems — FEI 3001726808

The FDA completed an inspection of Acist Medical Systems on March 4, 2019 in Eden Prairie, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 4, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Eden Prairie, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation