FDA inspection

Precision Interconnect, LLC: FDA inspection ending Sep 19, 2016

FDA inspection 986629 · Voluntary Action Indicated (VAI) · Wilsonville, OR

Key facts

Inspection ID 986629
Firm Precision Interconnect, LLC
FEI number 1000150964
Address 10025 SW Freeman Dr
City Wilsonville
State OR
ZIP 97070
Country United States
Fiscal year 2016
Inspection end date Sep 19, 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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