FDA inspection

ThyssenKrupp Access Corp: FDA inspection ending Aug 8, 2013

FDA inspection 843541 · No Action Indicated (NAI) · Grandview, MO

Key facts

Inspection ID 843541
Firm ThyssenKrupp Access Corp
FEI number 1925312
Address 4001 E 138th St
City Grandview
State MO
ZIP 64030
Country United States
Fiscal year 2013
Inspection end date Aug 8, 2013
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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