Home / Inspections / 979669

FDA Inspection 979669 — Abbott Diagnostics Scarborough, Inc.

Abbott Diagnostics Scarborough, Inc. — FEI 1221359

The FDA completed an inspection of Abbott Diagnostics Scarborough, Inc. on July 29, 2016 in Scarborough, ME. 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
July 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Scarborough, ME (United States)

Facility

Other inspections at this facility

  • 1074516 (VAI Fri Nov 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043498 (VAI Fri Mar 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820210 (NAI Fri Feb 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 725836 (NAI Fri May 20 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 598195 (VAI Fri Jul 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources