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FDA Inspection 1010178 — HTO Nevada Inc. dba Kirkman

HTO Nevada Inc. dba Kirkman — FEI 3004268965

The FDA completed an inspection of HTO Nevada Inc. dba Kirkman on April 14, 2017 in Lake Oswego, OR. 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
April 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lake Oswego, OR (United States)

Facility

Other inspections at this facility

  • 1279218 (OAI Fri Aug 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1216435 (VAI Thu Aug 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1083505 (VAI Fri Mar 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1065834 (NAI Mon Apr 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 935663 (NAI Wed Jul 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources