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FDA Inspection 1034270 — Radnostix

Radnostix — FEI 3003350319

The FDA completed an inspection of Radnostix on December 8, 2017 in Idaho Falls, ID. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 8, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Idaho Falls, ID (United States)

Facility

Other inspections at this facility

  • 1267869 (OAI Fri Apr 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1090194 (NAI Fri May 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 803415 (VAI Fri Oct 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 735266 (OAI Fri Jul 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources