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FDA Inspection 701865 — Risingsun Iodine Products Corp.

Risingsun Iodine Products Corp. — FEI 3005013963

The FDA completed an inspection of Risingsun Iodine Products Corp. on December 14, 2010 in Livingston, MT. 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 14, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Livingston, MT (United States)

Facility

Other inspections at this facility

  • 1238943 (VAI Thu Aug 29 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1171033 (NAI Wed Apr 13 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1127414 (NAI Thu Aug 06 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114120 (VAI Wed Nov 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767454 (OAI Thu Feb 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

  • Injunction (53) (Fri Nov 05 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources