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FDA Inspection 1074516 — Abbott Diagnostics Scarborough, Inc.

Abbott Diagnostics Scarborough, Inc. — FEI 1221359

The FDA completed an inspection of Abbott Diagnostics Scarborough, Inc. on November 30, 2018 in Scarborough, ME. 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
November 30, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Scarborough, ME (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1043498 (VAI Fri Mar 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979669 (NAI Fri Jul 29 2016 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