FDA inspection

LightScalpel, Inc.: FDA inspection ending Mar 13, 2019

FDA inspection 1083043 · No Action Indicated (NAI) · Bothell, WA

Key facts

Inspection ID 1083043
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 2019
Inspection end date Mar 13, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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