FDA inspection

R & D Medical Products, Inc.: FDA inspection ending Feb 3, 2010

FDA inspection 645184 · No Action Indicated (NAI) · Lake Forest, CA

Key facts

Inspection ID 645184
Firm R & D Medical Products, Inc.
FEI number 3001236548
Address 20492 Crescent Bay Dr Ste 106
City Lake Forest
State CA
ZIP 92630
Country United States
Fiscal year 2010
Inspection end date Feb 3, 2010
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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