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FDA Inspection 1068673 — Heartsine Technologies Inc

Heartsine Technologies Inc — FEI 3004018643

The FDA completed an inspection of Heartsine Technologies Inc on May 3, 2018 in Newtown, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 3, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newtown, PA (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 897171 (VAI Tue Sep 16 2014 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