FDA Inspection 1081356 — Acist Medical Systems

Acist Medical Systems — FEI 3001726808

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

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 4, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Eden Prairie, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.