FDA inspection

LightScalpel, Inc.: FDA inspection ending Jun 29, 2016

FDA inspection 976441 · Voluntary Action Indicated (VAI) · Bothell, WA

Key facts

Inspection ID 976441
Firm LightScalpel, Inc.
FEI number 3008720474
Address 11818 N Creek Pkwy N Ste 100
City Bothell
State WA
ZIP 98011
Country United States
Fiscal year 2016
Inspection end date Jun 29, 2016
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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