FDA inspection

Percussionaire Corporation: FDA inspection ending Mar 24, 2017

FDA inspection 1008842 · Voluntary Action Indicated (VAI) · Sandpoint, ID

Key facts

Inspection ID 1008842
Firm Percussionaire Corporation
FEI number 1000524541
Address 130 Mcghee Rd Ste 109
City Sandpoint
State ID
ZIP 83864
Country United States
Fiscal year 2017
Inspection end date Mar 24, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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