FDA inspection

Prestige Medical: FDA inspection ending Mar 10, 2010

FDA inspection 651875 · Voluntary Action Indicated (VAI) · Northridge, CA

Key facts

Inspection ID 651875
Firm Prestige Medical
FEI number 2081040
Address 8600 Wilbur Ave
City Northridge
State CA
ZIP 91324
Country United States
Fiscal year 2010
Inspection end date Mar 10, 2010
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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