FDA inspection

Rehabilicare: FDA inspection ending Mar 8, 2006

FDA inspection 416864 · No Action Indicated (NAI) · New Brighton, MN

Key facts

Inspection ID 416864
Firm Rehabilicare
FEI number 2126518
Address 1811 Old Highway 8 Nw
City New Brighton
State MN
ZIP 55112
Fiscal year 2006
Inspection end date Mar 8, 2006
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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