FDA inspection

Toomin Research Group: FDA inspection ending May 4, 2009

FDA inspection 579905 · No Action Indicated (NAI) · Los Angeles, CA

Key facts

Inspection ID 579905
Firm Toomin Research Group
FEI number 2024687
Address 6542 Hayes Dr
City Los Angeles
State CA
ZIP 90048
Country United States
Fiscal year 2009
Inspection end date May 4, 2009
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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