FDA inspection

Regenesis Biomedical Inc: FDA inspection ending Nov 9, 2011

FDA inspection 752842 · No Action Indicated (NAI) · Scottsdale, AZ

Key facts

Inspection ID 752842
Firm Regenesis Biomedical Inc
FEI number 3003070149
Address 5301 N Pima Rd Ste 150
City Scottsdale
State AZ
ZIP 85250
Country United States
Fiscal year 2012
Inspection end date Nov 9, 2011
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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