FDA inspection

Ameritek USA, Inc.: FDA inspection ending Jul 10, 2024

FDA inspection 1243511 · Voluntary Action Indicated (VAI) · Everett, WA

Key facts

Inspection ID 1243511
Firm Ameritek USA, Inc.
FEI number 1000126037
Address 125 130th St SE Ste 200
City Everett
State WA
ZIP 98208
Country United States
Fiscal year 2024
Inspection end date Jul 10, 2024
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
  • 10–99 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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