FDA inspection

Cleartooth Electronics, Inc.: FDA inspection ending Mar 17, 2016

FDA inspection 975851 · Voluntary Action Indicated (VAI) · Boulder, CO

Key facts

Inspection ID 975851
Firm Cleartooth Electronics, Inc.
FEI number 3008313821
Address 1025 S Monroe St
City Boulder
State CO
ZIP 80303
Country United States
Fiscal year 2016
Inspection end date Mar 17, 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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