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FDA Inspection 846664 — Prestige Medical

Prestige Medical — FEI 2081040

The FDA completed an inspection of Prestige Medical on August 28, 2013 in Northridge, CA. 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
August 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)

Facility

Other inspections at this facility

  • 1197590 (NAI Fri Jan 13 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1107415 (VAI Thu Oct 24 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 974724 (NAI Wed Jun 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 651875 (VAI Wed Mar 10 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources