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FDA Inspection 1049026 — Radiation Products Design,Inc

Radiation Products Design,Inc — FEI 2182762

The FDA completed an inspection of Radiation Products Design,Inc on April 10, 2018 in Albertville, MN. 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
April 10, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Albertville, MN (United States)

Facility

Other inspections at this facility

  • 1306546 (NAI Wed Mar 04 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 807050 (NAI Tue Nov 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 653205 (NAI Fri Mar 19 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources