FDA inspection

Rhythmia Medical Inc: FDA inspection ending Mar 25, 2015

FDA inspection 920097 · Voluntary Action Indicated (VAI) · Burlington, MA

Key facts

Inspection ID 920097
Firm Rhythmia Medical Inc
FEI number 3008438351
Address 111 S Bedford St Ste 205
City Burlington
State MA
ZIP 01803
Country United States
Fiscal year 2015
Inspection end date Mar 25, 2015
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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