FDA inspection

ACUTE Innovations LLC: FDA inspection ending Jan 28, 2016

FDA inspection 954923 · Voluntary Action Indicated (VAI) · Hillsboro, OR

Key facts

Inspection ID 954923
Firm ACUTE Innovations LLC
FEI number 3005670412
Address 8055 Ne Jacobson St Ste 700
City Hillsboro
State OR
ZIP 97124
Country United States
Fiscal year 2016
Inspection end date Jan 28, 2016
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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