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FDA Inspection 1151577 — Oscor Inc.

Oscor Inc. — FEI 1035166

The FDA completed an inspection of Oscor Inc. on September 10, 2021 in Palm Harbor, FL. 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 10, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Palm Harbor, FL (United States)

Facility

Other inspections at this facility

  • 1009131 (VAI Thu Mar 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 963563 (OAI Thu Mar 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 845108 (NAI Wed Aug 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 790329 (NAI Tue Jun 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 675299 (NAI Tue Jul 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources