FDA Inspection 1166885 — Acist Medical Systems

Acist Medical Systems — FEI 3001726808

The FDA completed an inspection of Acist Medical Systems on Feb 28, 2022 in Eden Prairie, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)

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