FDA inspection

Grand Medical: FDA inspection ending Mar 12, 2009

FDA inspection 570605 · Voluntary Action Indicated (VAI) · Kansas City, MO

Key facts

Inspection ID 570605
Firm Grand Medical
FEI number 3004873266
Address 8206 NW High Point Dr
City Kansas City
State MO
ZIP 64152
Country United States
Fiscal year 2009
Inspection end date Mar 12, 2009
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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