Home / Inspections / 897171

FDA Inspection 897171 — Heartsine Technologies Inc

Heartsine Technologies Inc — FEI 3004018643

The FDA completed an inspection of Heartsine Technologies Inc on September 16, 2014 in Newtown, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Newtown, PA (United States)

Facility

Other inspections at this facility

  • 1068673 (NAI Thu May 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847671 (OAI Thu Aug 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 652945 (NAI Tue Mar 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 601913 (OAI Tue Aug 04 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources