FDA inspection

Lerner Medical Devices Inc: FDA inspection ending Aug 10, 2011

FDA inspection 739949 · Voluntary Action Indicated (VAI) · Los Angeles, CA

Key facts

Inspection ID 739949
Firm Lerner Medical Devices Inc
FEI number 3006793564
Address 1545 Sawtelle Blvd Ste 36
City Los Angeles
State CA
ZIP 90025
Country United States
Fiscal year 2011
Inspection end date Aug 10, 2011
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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