FDA inspection

Unicare Biomedical, Inc.: FDA inspection ending May 9, 2013

FDA inspection 830902 · Voluntary Action Indicated (VAI) · Laguna Hills, CA

Key facts

Inspection ID 830902
Firm Unicare Biomedical, Inc.
FEI number 3003646540
Address 23011 Moulton Pkwy Ste J11
City Laguna Hills
State CA
ZIP 92653
Country United States
Fiscal year 2013
Inspection end date May 9, 2013
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
  • 10–99 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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