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FDA Inspection 989313 — Protek Medical Products Inc

Protek Medical Products Inc — FEI 3001701594

The FDA completed an inspection of Protek Medical Products Inc on October 6, 2016 in Coralville, IA. 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
October 6, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Coralville, IA (United States)

Facility

Other inspections at this facility

  • 1099061 (VAI Thu Aug 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 863555 (VAI Tue Jan 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 598379 (NAI Tue Jul 21 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources