FDA inspection

Acist Medical Systems: FDA inspection ending Mar 24, 2010

FDA inspection 654321 · No Action Indicated (NAI) · Eden Prairie, MN

Key facts

Inspection ID 654321
Firm Acist Medical Systems
FEI number 3001726808
Address 7905 Fuller Rd
City Eden Prairie
State MN
ZIP 55344
Country United States
Fiscal year 2010
Inspection end date Mar 24, 2010
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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