FDA inspection

Ortho Kinetics Corp: FDA inspection ending Sep 2, 2004

FDA inspection 342736 · Voluntary Action Indicated (VAI) · Vista, CA

Key facts

Inspection ID 342736
Firm Ortho Kinetics Corp
FEI number 1000160800
Address 2588 Progress St Ste 13
City Vista
State CA
ZIP 92081-8443
Fiscal year 2004
Inspection end date Sep 2, 2004
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med 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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