FDA inspection

Limerick Inc: FDA inspection ending Dec 7, 2012

FDA inspection 810442 · Voluntary Action Indicated (VAI) · Burbank, CA

Key facts

Inspection ID 810442
Firm Limerick Inc
FEI number 3002297831
Address 2150 N Glenoaks Blvd
City Burbank
State CA
ZIP 91504
Country United States
Fiscal year 2013
Inspection end date Dec 7, 2012
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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