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FDA Inspection 843058 — Abbott Medical

Abbott Medical — FEI 2017865

The FDA completed an inspection of Abbott Medical on August 1, 2013 in Sylmar, CA. 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
August 1, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Sylmar, CA (United States)

Facility

Other inspections at this facility

  • 1209394 (VAI Wed Jun 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1120476 (NAI Fri Jan 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099418 (VAI Fri Aug 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1000696 (OAI Fri Feb 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 964165 (NAI Thu Mar 24 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources