FDA inspection

Kustomer Kinetics, Inc.: FDA inspection ending Jun 15, 2010

FDA inspection 667224 · Voluntary Action Indicated (VAI) · Arcadia, CA

Key facts

Inspection ID 667224
Firm Kustomer Kinetics, Inc.
FEI number 1418327
Address 136 E Saint Joseph St Ste A
City Arcadia
State CA
ZIP 91006
Country United States
Fiscal year 2010
Inspection end date Jun 15, 2010
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • None 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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